US6211294B1 - Multicomponent fiber prepared from a thermoplastic composition - Google Patents

Multicomponent fiber prepared from a thermoplastic composition Download PDF

Info

Publication number
US6211294B1
US6211294B1 US09/222,094 US22209498A US6211294B1 US 6211294 B1 US6211294 B1 US 6211294B1 US 22209498 A US22209498 A US 22209498A US 6211294 B1 US6211294 B1 US 6211294B1
Authority
US
United States
Prior art keywords
polymer
polybutylene succinate
weight percent
fiber
thermoplastic composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
US09/222,094
Inventor
Fu-Jya Tsai
Brian T. Etzel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US09/222,094 priority Critical patent/US6211294B1/en
Priority to US09/372,019 priority patent/US6207755B1/en
Priority to US09/436,682 priority patent/US6201068B1/en
Priority to US09/437,026 priority patent/US6268434B1/en
Priority to US09/606,571 priority patent/US6475418B1/en
Application granted granted Critical
Publication of US6211294B1 publication Critical patent/US6211294B1/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D01NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
    • D01FCHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
    • D01F6/00Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof
    • D01F6/88Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds
    • D01F6/92Monocomponent artificial filaments or the like of synthetic polymers; Manufacture thereof from mixtures of polycondensation products as major constituent with other polymers or low-molecular-weight compounds of polyesters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/15203Properties of the article, e.g. stiffness or absorbency
    • A61F13/15252Properties of the article, e.g. stiffness or absorbency compostable or biodegradable
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/22Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons containing macromolecular materials
    • A61L15/225Mixtures of macromolecular compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61LMETHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
    • A61L15/00Chemical aspects of, or use of materials for, bandages, dressings or absorbent pads
    • A61L15/16Bandages, dressings or absorbent pads for physiological fluids such as urine or blood, e.g. sanitary towels, tampons
    • A61L15/42Use of materials characterised by their function or physical properties
    • A61L15/62Compostable, hydrosoluble or hydrodegradable materials
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/02Polyesters derived from dicarboxylic acids and dihydroxy compounds
    • C08L67/03Polyesters derived from dicarboxylic acids and dihydroxy compounds the dicarboxylic acids and dihydroxy compounds having the carboxyl- and the hydroxy groups directly linked to aromatic rings
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L67/00Compositions of polyesters obtained by reactions forming a carboxylic ester link in the main chain; Compositions of derivatives of such polymers
    • C08L67/04Polyesters derived from hydroxycarboxylic acids, e.g. lactones
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H1/00Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
    • D04H1/40Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
    • D04H1/42Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties characterised by the use of certain kinds of fibres insofar as this use has no preponderant influence on the consolidation of the fleece
    • D04H1/4382Stretched reticular film fibres; Composite fibres; Mixed fibres; Ultrafine fibres; Fibres for artificial leather
    • D04H1/43825Composite fibres
    • DTEXTILES; PAPER
    • D04BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
    • D04HMAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
    • D04H3/00Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length
    • D04H3/08Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating
    • D04H3/16Non-woven fabrics formed wholly or mainly of yarns or like filamentary material of substantial length characterised by the method of strengthening or consolidating with bonds between thermoplastic filaments produced in association with filament formation, e.g. immediately following extrusion
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2300/00Characterised by the use of unspecified polymers
    • C08J2300/22Thermoplastic resins
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2201/00Properties
    • C08L2201/06Biodegradable
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2205/00Polymer mixtures characterised by other features
    • C08L2205/02Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249924Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
    • Y10T428/24994Fiber embedded in or on the surface of a polymeric matrix
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249924Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
    • Y10T428/24994Fiber embedded in or on the surface of a polymeric matrix
    • Y10T428/249941Fiber is on the surface of a polymeric matrix having no embedded portion
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249924Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
    • Y10T428/24994Fiber embedded in or on the surface of a polymeric matrix
    • Y10T428/249942Fibers are aligned substantially parallel
    • Y10T428/249947Polymeric fiber
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249924Noninterengaged fiber-containing paper-free web or sheet which is not of specified porosity
    • Y10T428/24994Fiber embedded in or on the surface of a polymeric matrix
    • Y10T428/24995Two or more layers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2904Staple length fiber
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/29Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
    • Y10T428/2913Rod, strand, filament or fiber
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31786Of polyester [e.g., alkyd, etc.]

Definitions

  • the present invention relates to a thermoplastic composition.
  • the thermoplastic composition comprises an unreacted mixture of a poly(lactic acid) polymer, a polybutylene succinate polymer or a polybutylene succinate adipate polymer or a mixture of such polymers, and a wetting agent.
  • the thermoplastic composition exhibits substantial biodegradable properties yet is easily processed.
  • the thermoplastic composition is useful in making multicomponent fibers or nonwoven structures that may be used in a disposable absorbent product intended for the absorption of fluids such as body fluids.
  • Disposable absorbent products currently find widespread use in many applications. For example, in the infant and child care areas, diapers and training pants have generally replaced reusable cloth absorbent articles.
  • Other typical disposable absorbent products include feminine care products such as sanitary napkins or tampons, adult incontinence products, and health care products such as surgical drapes or wound dressings.
  • a typical disposable absorbent product generally comprises a composite structure including a topsheet, a backsheet, and an absorbent structure between the topsheet and backsheet. These products usually include some type of fastening system for fitting the product onto the wearer.
  • Disposable absorbent products are typically subjected to one or more liquid insults, such as of water, urine, menses, or blood, during use.
  • the outer cover backsheet materials of the disposable absorbent products are typically made of liquid-insoluble and liquid impermeable materials, such as polypropylene films, that exhibit a sufficient strength and handling capability so that the disposable absorbent product retains its integrity during use by a wearer and does not allow leakage of the liquid insulting the product.
  • the outer cover materials are made very thin in order to reduce the overall bulk of the disposable absorbent product so as to reduce the likelihood of blockage of a toilet or a sewage pipe, then the outer cover material typically will not exhibit sufficient strength to prevent tearing or ripping as the outer cover material is subjected to the stresses of normal use by a wearer.
  • the disposable absorbent product may be easily and efficiently disposed of by composting.
  • the disposable absorbent product may be easily and efficiently disposed of to a liquid sewage system wherein the disposable absorbent product is capable of being degraded.
  • degradable monocomponent fibers are known, problems have been encountered with their use.
  • known degradable fibers typically do not have good thermal dimensional stability such that the fibers usually undergo severe heat-shrinkage due to the polymer chain relaxation during downstream heat treatment processes such as thermal bonding or lamination.
  • poly(lactic acid) polymers are known to have a relatively slow crystallization rate as compared to, for example, polyolefin polymers, thereby often resulting in poor processability of the aliphatic polyester polymers.
  • the poly(lactic acid) polymers generally do not have good thermal dimensional-stability.
  • the poly(lactic acid) polymers usually undergo severe heat-shrinkage due to the relaxation of the polymer chain during downstream heat treatment processes, such as thermal bonding and lamination, unless an extra step such as heat setting is taken.
  • heat setting step generally limits the use of the fiber in in-situ nonwoven forming processes, such as spunbond and meltblown, where heat setting is very difficult to be accomplished.
  • thermoplastic composition which exhibits desired processability, liquid wettability, and thermal dimensional-stability properties.
  • thermoplastic composition which may be easily and efficiently formed into a fiber.
  • thermoplastic composition which is suitable for use in preparing nonwoven structures.
  • the present invention concerns a thermoplastic composition that is substantially biodegradable and yet which is easily prepared and readily processable into desired final structures, such as fibers or nonwoven structures.
  • thermoplastic composition that comprises a mixture of a first component, a second component, and a third component.
  • thermoplastic composition comprises an unreacted mixture of a poly(lactic acid) polymer; a polybutylene succinate polymer or a polybutylene succinate adipate polymer or a mixture of such polymers; and a wetting agent for the poly(lactic acid) polymer, the polybutylene succinate polymer or the polybutylene succinate adipate polymer or a mixture of such polymers.
  • the present invention concerns a multicomponent fiber that is substantially degradable and yet which is easily prepared and readily processable into desired final structures, such nonwoven structures.
  • One aspect of the present invention concerns a multicomponent fiber that comprises an unreacted mixture of a poly(lactic acid) polymer; a polybutylene succinate polymer or a polybutylene succinate adipate polymer or a mixture of such polymers; and a wetting agent for the aliphatic polyester polymer and the polybutylene succinate polymer or the polybutylene succinate adipate polymer or a mixture of such polymers.
  • the present invention concerns a nonwoven structure comprising the multicomponent fiber disclosed herein.
  • One embodiment of such a nonwoven structure is a frontsheet useful in a disposable absorbent product.
  • the present invention concerns a process for preparing the multicomponent fiber disclosed herein.
  • the present invention concerns a disposable absorbent product comprising the multicomponent fiber disclosed herein.
  • thermoplastic is meant to refer to a material that softens when exposed to heat and substantially returns to its original condition when cooled to room temperature.
  • thermoplastic composition may be prepared wherein such thermoplastic composition is substantially degradable yet which thermoplastic composition is easily processed into fibers and nonwoven structures that exhjbit effective fibrous mechanical properties.
  • the first component in the thermoplastic composition is poly(lactic acid) polymer.
  • Poly(lactic add) polymer is generally prepared by the polymerization of lactic acid.
  • a chemically equivalent material may also be prepared by the polymerization of lactide.
  • poly(lactic acid) polymer is intended to represent the polymer that is prepared by either the polymerization of lactic acid or lactide.
  • Lactic acid and lactide are known to be asymmetrical molecules, having two optical isomers referred to, respectively, as the levorotatory (hereinafter referred to as “L”) enantiomer and the dextrorotatory (hereinafter referred to as “D”) enantiomer.
  • L levorotatory
  • D dextrorotatory
  • thermoplastic composition By being able to control such properties, it is possible to prepare a thermoplastic composition and a multicomponent fiber exhibiting desired melt strength, mechanical properties, softness, and processability properties so as to be able to make attenuated, heat-set, and crimped fibers.
  • the poly(lactic acid) polymer be present in the thermoplastic composition in an amount effective to result in the thermoplastic composition exhibiting desired properties.
  • the poly(lactic acid) polymer will be present in the thermoplastic composition in a weight amount that is greater than 0 but less than 100 weight percent, beneficially between about 5 weight percent to about 95 weight percent, suitably between about 10 weight percent to about 90 weight percent, and more suitably between about 15 weight percent to about 85 weight percent, wherein all weight percents are based on the total weight amount of the poly(lactic acid) polymer, the polybutylene succinate polymer or polybutylene succinate adipate polymer or a mixture of such polymers, and the wetting agent present in the thermoplastic composition.
  • the compositional ratio of the three components in the thermoplastic composition is generally important to obtain the desired properties of the thermoplastic composition, such as wettability, biodegradability, thermal stability and processability.
  • the second component in the thermoplastic composition is a polybutylene succinate polymer, a polybutylene succinate adipate polymer, or a mixture of such polymers.
  • a polybutylene succinate polymer is generally prepared by the condensation polymerization of a glycol and a dicarboxylic acid or an acid anhydride thereof.
  • a polybutylene succinate polymer may either be a linear polymer or a long-chain branched polymer.
  • a long-chain branched polybutylene succinate polymer is generally prepared by using an additional polyfunctional component selected from the group consisting of trifunctional or tetrafunctional polyols, oxycarboxylic acids, and polybasic carboxylic acids.
  • Polybutylene succinate polymers are known in the art and are described, for example, in European Patent Application 0 569 153 A2 to Showa Highpolymer Co., Ltd., Tokyo, Japan.
  • a polybutylene succinate adipate polymer is generally prepared by the polymerization of at least one alkyl glycol and more than one aliphatic multifunctional acid.
  • Polybutylene succinate adipate polymers are also known in the art.
  • polybutylene succinate polymers and polybutylene succinate adipate polymers that are suitable for use in the present invention include a variety of polybutylene succinate polymers and polybutylene succinate adipate polymers that are available from Showa Highpolymer Co., Ltd., Tokyo, Japan, under the designation Bionolle 1903 polybutylene succinate polymer, with long chain branches, or Bionolle 1020 polybutylene succinate polymer, which is an essentially linear polymer.
  • the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers be present in the thermoplastic composition in an amount effective to result in the thermoplastic composition exhibiting desired properties.
  • the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers will be present in the thermoplastic composition in a weight amount that is greater than 0 but less than 100 weight percent, beneficially between about 5 weight percent to about 95 weight percent, suitably between about 10 weight percent to about 90 weight percent, and more suitably between about 15 weight percent to about 85 weight percent, wherein all weight percents are based on the total weight amount of The poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent present in the thermoplastic composition.
  • the poly(lactic acid) polymer and the polybutylene succinate polymer and/or the polybutylene succinate adipate polymer exhibit a weight average molecular weight that is effective for the thermoplastic composition to exhibit desirable melt strength, fiber mechanical strength, and fiber spinning properties.
  • the weight average molecular weight of a particular polymer is too high, this represents that the polymer chains are heavily entangled which may result in a thermoplastic composition comprising that polymer being difficult to process.
  • the weight average molecular weight of a particular polymer is too low, this represents that the polymer chains are not entangled enough which may result in a thermoplastic composition comprising that polymer exhibiting a relatively weak melt strength, making high speed processing very difficult.
  • poly(lactic acid) polymers, polybutylene succinate polymers, and/or polybutylene succinate adipate polymers suitable for use in the present invention respectively exhibit weight average molecular weights that are beneficially between about 10,000 to about 2,000,000, more beneficially between about 50,000 to about 400,000, and suitably between about 100,000 to about 300,000.
  • the weight average molecular weight for polymers or polymer blends can be determined using a method as described in the Test Methods section herein.
  • polydispersity index is meant to represent the value obtained by dividing the weight average molecular weight of a polymer by the number average molecular weight of the polymer. In general, if the polydispersity index value of a particular polymer is too high, a thermoplastic composition comprising that polymer may be difficult to process due to inconsistent processing properties caused by polymer segments comprising low molecular weight polymers that have lower melt strength properties during spinning.
  • the poly(lactic acid) polymer, the polybutylene succinate polymer, and/or the polybutylene succinate adipate polymer respectively exhibit a polydispersity index value that is beneficially between about 1 to about 15, more beneficially between about 1 to about 4, and suitably between about 1 to about 3.
  • the number average molecular weight for polymers or polymer blends can be determined using a method as described in the Test Methods section herein.
  • the poly(lactic acid) polymer, the olybutylene succinate polymer, and the polybutylene succinate adipate polymer be biodegradable.
  • the thermoplastic composition comprising these polymers either in the form of a fiber or in the form of a nonwoven structure, will be substantially degradable when disposed of to the environment and exposed to air and/or water.
  • biodegradable is meant to represent that a material degrades from the action of naturally occurring microorganisms such as bacteria, fungi, and algae.
  • the poly(lactic acid) polymer, the polybutylene succinate polymer, and the polybutylene succinate adipate polymer be compostable.
  • the thermoplastic composition comprising these polymers either in the form of a fiber or in the form of a nonwoven structure, will be substantially compostable when disposed of to the environment and exposed to air and/or water.
  • compostable is meant to represent that a material is capable of undergoing biological decomposition in a compost site such that the material is not visually distinguishable and breaks down into carbon dioxide, water, inorganic compounds, and biomass, at a rate consistent with known compostable materials.
  • hydrophobic refers to a material having a contact angle of water in air of at least 90 degrees.
  • hydroophilic refers to a material having a contact angle of water in air of less than 90 degrees.
  • the poly(lactic acid) polymer, the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers be melt processable. It is therefore desired that the polymers used in the present invention exhibit a melt flow rate that is beneficially between about 1 gram per 10 minutes to about 600 grams per 10 minutes, suitably between about 5 grams per 10 minutes to about 200 grams per 10 minutes, and more suitably between about 10 grams per 10 minutes to about 150 grams per 10 minutes.
  • the melt flow rate of a material may be determined according to ASTM Test Method D1238-E, incorporated in its entirety herein by reference.
  • fiber or “fibrous” is meant to refer to a material wherein the length to diameter ratio of such material is greater than about 10.
  • a “nonfiber” or “nonfibrous” material is meant to refer to a material wherein the length to diameter ratio of such material is about 10 or less.
  • the poly(lactic acid) polymer and the polybutylene succinate polymer and/or the polybutylene succinate adipate polymer are generally hydrophobic. Since it is desired that the thermoplastic composition of the present invention, and fibers prepared from the thermoplastic composition, generally be hydrophilic, it has been found that there is a need for the use of another component in the thermoplastic composition of the present invention in order to achieve the desired properties.
  • poly(lactic acid) polymer and the polybutylene succinate polymer and/or the polybutylene succinate adipate
  • such polymers are not chemically identical and are, therefore, somewhat incompatible with each other which negatively affects the processing of a mixture of such polymers.
  • the poly(lactic acid) polymer, the polybutylene succinate polymer, and/or the polybutylene succinate adipate polymer are sometimes difficult to effectively mix and prepare as an essentially homogeneous mixture on their own.
  • the present invention generally requires the use of a wetting agent that allows for the effective preparation and processing of the poly(lactic acid) polymer, the polybutylene succinate polymer, and/or the polybutylene succinate adipate polymer into a single thermoplastic composition.
  • the third component in the thermoplastic composition is a wetting agent for the poly(lactic acid) polymer and the polybutylene succinate polymer and/or the polybutylene succinate adipate polymer.
  • Wetting agents suitable for use in the present invention will generally comprise a hydrophilic section which will generally be compatible to poly(lactic acid) polymer and the hydrophilic sections of polybutylene succinate polymer or polybutylene succinate adipate polymer and a hydrophobic section which will generally be compatible to the hydrophobic sections of polybutylene succinate polymer or polybutylene succinate adipate polymer.
  • These hydrophilic and hydrophobic sections of the wetting agent will generally exist in separate blocks so that the overall wetting agent structure may be di-block or random block.
  • the wetting agent initially functions as a plasticizer and an agent to enhance cohesion between the different polymers in order to improve the preparation and processing of the thermoplastic composition. It is then generally desired that the wetting agent then serves as a surfactant in a material processed from the thermoplastic composition, such as a fiber or nonwoven structure, by modifying the contact angle of water in air of the processed material.
  • the hydrophobic portion of the wetting agent may be, but is not limited to, a polyolefin such as polyethylene or polypropylene.
  • the hydrophilic portion of the wetting agent may contain ethylene oxide, ethoxylates, glycols, alcohols or any combinations thereof. Examples of suitable wetting agents include UNITHOX® 480 and UNITHOX® 0750 ethoxylated alcohols, or UNICID® Acid Amide Ethoxylates, all available from Petrolite Corporation of Tulsa, Okla.
  • the wetting agent exhibit a weight average molecular weight that is effective for the thermoplastic composition to exhibit desirable melt strength, fiber mechanical strength, and fiber spinning properties.
  • the weight average molecular weight of a wetting agent is too high, the wetting agent will not blend well with the other components in the thermoplastic composition because the wetting agent's viscosity will be so high that it lacks the mobility needed to blend.
  • the weight average molecular weight of the wetting agent is too low, this represents that the wetting agent will generally not blend well with the other components and have such a low viscosity that it causes processing problems.
  • wetting agents suitable for use in the present invention exhibit weight average molecular weights that are beneficially between about 1,000 to about 100,000, suitably between about 1,000 to about 50,000, and more suitably between about 1,000 to about 10,000.
  • the weight average molecular weight for a material can be determined using a method as described in the Test Methods section herein.
  • the wetting agent exhibit an effective hydrophilic-lipophilic balance ratio (HLB ratio).
  • HLB ratio of a material describes the relative ratio of the hydrophilicity of the material.
  • the HLB ratio is calculated as the weight average molecular weight of the hydrophilic portion divided by the total weight average molecular weight of the material, which value is then multiplied by 20. If the HLB ratio value is too low, the wetting agent will generally not provide the desired improvement in hydrophilicity. Conversely, if the HLB ratio value is too high, the wetting agent will not blend into the thermoplastic composition because of chemical incompatibility and differences in viscosities with the other components.
  • wetting agents useful in the present invention exhibit HLB ratio values that are beneficially between about 10 to about 40, suitably between about 10 to about 20, and more suitably between about 12 to about 16.
  • the wetting agent be present in the thermoplastic composition in an amount effective to result in the thermoplastic composition exhibiting desired properties such as desirable heat shrinkage and desirable contact angle values.
  • a minimal amount of the wetting agent will be needed to achieve an effective blending and processing with the other components in the thermoplastic composition.
  • too much of the compatibilizer may lead to processing problems of the thermoplastic composition or to a final thermoplastic composition that does not exhibit desired properties such as desired advancing and receding contact angle values.
  • the wetting agent will be present in the thermoplastic composition in a weight amount that is greater than 0 to about 15 weight percent, beneficially between about 0.5 weight percent to about 15 weight percent, more beneficially between about I weight percent to about 13 weight percent, suitably between about 1 weight percent to about 10 weight percent, and more suitably between about 1 weight percent to about 5 weight percent, wherein all weight percents are based on the total weight amount of the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent present in the thermoplastic composition.
  • thermoplastic composition of the present invention
  • thermoplastic composition is not limited thereto and can include other components not adversely effecting the desired properties of the thermoplastic composition.
  • Exemplary materials which could be used as additional components would include, without limitation, pigments, antioxidants, stabilizers, surfactants, waxes, flow promoters, solid solvents, plasticizers, nucleating agents, particulates, and other materials added to enhance the processability of the thermoplastic composition.
  • additional components are included in a thermoplastic composition, it is generally desired that such additional components be used in an amount that is beneficially less than about 10 weight percent, more beneficially less than about 5 weight percent, and suitably less than about 1 weight percent, wherein all weight percents are based on the total weight amount of the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent present in the thermoplastic composition.
  • the thermoplastic composition of the present invention is generally simply a mixture of the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; the wetting agent, and, optionally, any additional components.
  • it is desirable that the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent remain substantially unreacted with each other.
  • each of the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent remain distinct components of the thermoplastic composition.
  • each of the poly(lactic acid) polymer and the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers will generally form separate regions or domains within a prepared mixture forming the thermoplastic composition.
  • an essentially continuous phase may be formed from the polymer that is present in the thermoplastic composition in a relatively greater amount.
  • the polymer that is present in the thermoplastic composition in a relatively lesser amount may form an essentially discontinuous phase, forming separate regions or domains within the continuous phase of the more prevalent polymer wherein the more prevalent polymer continuous phase substantially encases the less prevalent polymer within its structure.
  • the term “encase”, and related terms are intended to mean that the more prevalent polymer continuous phase substantially encloses or surrounds the less prevalent polymer's separate regions or domains.
  • thermoplastic composition or a multicomponent fiber of the present invention it is desired that the poly(lactic acid) polymer form an essentially continuous phase and that the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers form an essentially discontinuous phase, wherein the poly(lactic acid) polymer substantially encases regions or domains of the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers.
  • the poly(lactic acid) polymer is present in the thermoplastic composition or multicomponent fiber in a weight amount that is between about 75 weight percent to about 90 weight percent and that the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers is present in the thermoplastic composition or multicomponent fiber in a weight amount that is between about 5 weight percent to about 20 weight percent, wherein all weight percents are based on the total weight amount of the poly(lactic acid) polymer, the polybutylene succinate polymer or polybutylene succinate adipate polymer or a mixture of such polymers, and the wetting agent present in the thermoplastic composition or the multicomponent fiber.
  • thermoplastic composition dry mixture is beneficially agitated, stirred, or otherwise blended to effectively uniformly mix the poly(lactic acid) polymer, the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent such that an essentially homogeneous dry mixture is formed.
  • the dry mixture may then be melt blended in, for example, an extruder, to effectively uniformly mix the poly(lactic acid) polymer, the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent such that an essentially homogeneous melted mixture is formed.
  • the essentially homogeneous melted mixture may then be cooled and pelletized. Altematively, the essentially homogeneous melted mixture may be sent directly to a spin pack or other equipment for forming fibers or a nonwoven structure.
  • Alternative methods of mixing together the components of the present invention include first mixing together the poly(lactic acid) polymer and the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers and then adding the wetting agent to such a mixture in, for example, an extruder being used to mix the components together. In addition, it is also possible to initially melt mix all of the components together at the same time. Other methods of mixing together the components of the present invention are also possible and will be easily recognized by one skilled in the art.
  • the present invention is also directed to a multicomponent fiber which is prepared from the thermoplastic composition of the present invention.
  • a multicomponent fiber comprising only three components.
  • the scope of the present invention is meant to include fibers with three or more components.
  • thermoplastic composition of the present invention When the thermoplastic composition of the present invention is formed into a multicomponent fiber, an exposed surface on at least a portion of the multicomponent fiber will typically be formed from the more prevalent polymer present in the multicomponent fiber. Such an exposed surface on at least a portion of the multicomponent fiber which will generally permit thermal bonding of the multicomponent fiber to other fibers which may be the same or different from the multicomponent fiber of the present invention. As a result, the multicomponent fiber can then be used to form thermally bonded fibrous nonwoven structures such as a nonwoven web.
  • Typical conditions for thermally processing the various components indude using a shear rate that is beneficially between about 100 seconds ⁇ 1 to about 50000 seconds ⁇ 1 , more beneficially between about 500 seconds ⁇ 1 to about 5000 seconds ⁇ 1 , suitably between about 1000 seconds ⁇ 1 to about 3000 seconds ⁇ 1 , and most suitably at about 1000 seconds ⁇ 1 .
  • Typical conditions for thermally processing the components also include using a temperature that is beneficially between about 100° C. to about 500° C., more beneficially between about 150° C. to about 300 °C, and suitably between about 175° C. to about 250° C.
  • the melt spinning of polymers includes the production of continuous filament, such as spunbond or meltblown, and non-continuous filament, such as staple and shortcut fibers.
  • a thermoplastic composition is extruded and fed to a distribution system where the thermoplastic composition is introduced into a spinneret plate.
  • the spun fiber is then cooled, solidified, and drawn by an aerodynamic system, to be formed into a conventional nonwoven.
  • the spun fiber is cooled, solidified, and drawn, generally by a mechanical rolls system, to an intermediate filament diameter and collected. Subsequently, the fiber may be “cold drawn” at a temperature below its softening temperature, to the desired finished fiber diameter and crimped or texturized and cut into a desirable fiber length.
  • Multicomponent fibers can be cut into relatively short lengths, such as staple fibers which generally have lengths in the range of about 25 to about 50 millimeters and short-cut fibers which are even shorter and generally have lengths less than about 18 millimeters.
  • the resultant multicomponent fibers of the present invention are desired to exhibit an improvement in hydrophilicity, evidenced by a decrease in the contact angle of water in air.
  • the contact angle of water in air of a fiber sample can be measured as either an advancing or a receding contact angle value because of the nature of the testing procedure.
  • the advancing contact angle measures a material's initial response to a liquid, such as water.
  • the receding contact angle gives a measure of how a material will perform over the duration of a first insult, or exposure to liquid, as well as over following insults.
  • a lower receding contact angle means that the material is becoming more hydrophilic during the liquid exposure and will generally then be able to transport liquids more consistently.
  • Both the advancing and receding contact angle data is desirably used to establish the highly hydrophilic nature of a multicomponent fiber of the present invention.
  • the multicomponent fiber exhibits an Advancing Contact Angle value that is beneficially less than about 80 degrees, more beneficially less than about 75 degrees, suitably less than about 70 degrees, more suitably less than about 60 degrees, and most suitably less than about 50 degrees, wherein the Advancing Contact Angle value is determined by the method that is described in the Test Methods section herein.
  • the multicomponent fiber exhibits a Receding Contact Angle value that is beneficially less than about 60 degrees, more beneficially less than about 55 degrees, suitably less than about 50 degrees, more suitably less than about 45 degrees, and most suitably less than about 40 degrees, wherein the Receding Contact Angle value is determined by the method that is described in the Test Methods section herein.
  • the difference between the Advancing Contact Angle value and the Receding Contact Angle value commonly known as the contact angle hysteresis, be as small as possible.
  • the multicomponent fiber exhibits a difference between the Advancing Contact Angle value and the Receding Contact Angle value that is beneficially less than about 30 degrees, more beneficially less than about 25 degrees, suitably less than about 20 degrees, and more suitably less than about 10 degrees.
  • Typical poly(lactic acid) polymer materials often undergo heat shrinkage during downstream thermal processing.
  • the heat-shrinkage mainly occurs due to the thermally-induced chain relaxation of the polymer segments in the amorphous phase and incomplete crystalline phase.
  • the typical solution to this problem is to subject the material to a heat-setting treatment. As such, when prepared materials, such as fibers, are subjected to heat-setting upon reaching a bonding roll, the fibers won't substantially shrink because such fibers are already fully or highly oriented.
  • the present invention alleviates the need for this additional processing step because of the composition of the multicomponent fiber of the present invention.
  • the addition of the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers, and the wetting agent decrease the heat shrinkage of a multicomponent fiber as compared to a fiber that is prepared from only poly(lactic acid) polymer.
  • the multicomponent fiber exhibit an amount of shrinking, at a temperature of about 90° C., that is beneficially less than about 15 percent, more beneficially less than about 10 percent, and suitably less than about 5 percent, wherein the amount of shrinking is based upon the difference between the initial and final lengths of the fiber divided by the initial length of the fiber multiplied by 100.
  • the method by which the amount of shrinking that a fiber exhibits may be determined is included in the Test Methods section herein.
  • the multicomponent fiber exhibit an amount of shrinking, suitably less than about 5 percent at a temperature of about 90° C., that results in a nonwoven structure formed from the multicomponent fiber to exhibit a quilting or waviness effect that increases the surface area of the nonwoven structure since the shrinking of the multicomponent fibers causes the nonwoven structure to exhibit a three dimensional topography.
  • a quilting or waviness effect of the nonwoven structure has been found to improve the softness and z-directional transport of a liquid within the nonwoven structure.
  • multicomponent fibers also exhibit desired mechanical strength properties, such as a break stress value as well as a modulus value, such that the multicomponent fibers maintain their integrity during use.
  • a multicomponent fiber prepared from the thermoplastic composition of the present invention exhibits an improved break stress value as well as an improved modulus value as compared to a fiber that is prepared solely from poly(lactic acid) polymer.
  • a multicomponent fiber prepared from the thermoplastic composition of the present invention exhibits a break stress value that is at least twice the break stress value exhibited by an otherwise identical fiber that is prepared solely from the poly(lactic acid) polymer used to prepare the multicomponent fiber.
  • the multicomponent fiber exhibit a break stress value that is greater than about 10 MPa, beneficially greater than about 15 MPa, suitably greater than about 20 MPa, and up to about 100 MPa.
  • the multicomponent fiber exhibit a modulus value that is less than about 150 MPa, beneficially less than about 125 MPa, and suitably less than about 100 MPa.
  • the multicomponent fibers of the present invention are suited for use in disposable products including disposable absorbent products such as diapers, adult incontinent products, and bed pads; in catamenial devices such as sanitary napkins, and tampons; and other absorbent products such as wipes, bibs, wound dressings, and surgical capes or drapes. Accordingly, in another aspect, the present invention relates to a disposable absorbent product comprising the multicomponent fibers of the present invention.
  • the multicomponent fibers are formed into a fibrous matrix for incorporation into a disposable absorbent product.
  • a fibrous matrix may take the form of, for example, a fibrous nonwoven web. Fibrous nonwoven webs may be made completely from the multicomponent fibers of the present invention or they may be blended with other fibers.
  • the length of the fibers used may depend on the particular end use contemplated. Where the fibers are to be degraded in water as, for example, in a toilet, it is advantageous if the lengths are maintained at or below about 15 millimeters.
  • a disposable absorbent product comprises a liquid-permeable topsheet, a backsheet attached to the liquid-permeable topsheet, and an absorbent structure positioned between the liquid-permeable topsheet and the backsheet, wherein the liquid-permeable topsheet comprises multicomponent fibers of the present invention.
  • Absorbent products and structures according to all aspects of the present invention are generally subjected, during use, to multiple insults of a body liquid. Accordingly, the absorbent products and structures are desirably capable of absorbing multiple insults of body liquids in quantities to which the absorbent products and structures will be exposed during use. The insults are generally separated from one another by a period of time.
  • the melting temperature of a material was determined using differential scanning calorimetry.
  • a differential scanning calorimeter under the designation Thermal Analyst 2910 Differential Scanning Calorimeter, which was outfitted with a liquid nitrogen cooling accessory and used in combination with Thermal Analyst 2200 analysis software (version 8.10) program, both available from T.A. Instruments Inc. of New Castle, Del., was used for the determination of melting temperatures.
  • the material samples tested were either in the form of fibers or resin pellets. It is preferred to not handle the material samples directly, but rather to use tweezers and other tools, so as not to introduce anything that would produce erroneous results.
  • the material samples were cut, in the case of fibers, or placed, in the case of resin pellets, into an aluminum pan and weighed to an accuracy of 0.01 mg on an analytical balance. If needed, a lid was crimped over the material sample onto the pan.
  • the differential scanning calorimeter was calibrated using an indium metal standard and a baseline correction performed, as described in the manual for the differential scanning calorimeter.
  • a material sample was placed into the test chamber of the differential scanning calorimeter for testing and an empty pan is used as a reference. All testing was run with a 55 cubic centimeter/minute nitrogen (industrial grade) purge on the test chamber.
  • the heating and cooling program is a 2 cycle test that begins with equilibration of the chamber to ⁇ 75° C., followed by a heating cycle of 20° C./minute to 220° C., followed by a cooling cycle at 20° C./minute to ⁇ 75° C., and then another heating cyde of 20° C./minute to 220° C.
  • Tg glass transition temperature
  • a capillary rheometer under the designation Göttfert Rheograph 2003 capillary rheometer, which was used in combination with WinRHEO (version 2.31) analysis software, both available from Göttfert Company of Rock Hill, S.C., was used to evaluate the apparent viscosity rheological properties of material samples.
  • the capillary rheometer setup included a 2000 bar pressure transducer and a 30 mm length/30 mm active length/1 mm diameter/0 mm height180° run in angle, round hole capillary die.
  • the material sample being tested demonstrates or is known to have water sensitivity
  • the material sample is dried in a vacuum oven above its glass transition temperature, i.e. above 55 or 60° C. for poly(lactic acid) materials, under a vacuum of at least 15 inches of mercury with a nitrogen gas purge of at least 30 standard cubic feet per hour for at least 16 hours.
  • the material sample is loaded incrementally into the column, packing resin into the column with a ramrod each time to ensure a consistent melt during testing.
  • a 2 minute melt time precedes each test to allow the material sample to completely melt at the test temperature.
  • the capillary rheometer takes data points automatically and determines the apparent viscosity (in Pascal. second) at 7 apparent shear rates (in second ⁇ 1 ): 50, 100, 200, 500, 1000, 2000, and 5000.
  • apparent viscosity in Pascal. second
  • apparent shear rates in second ⁇ 1
  • the resultant rheology curve of apparent shear rate versus apparent viscosity gives an indication of how the material sample will run at that temperature in an extrusion process.
  • the apparent viscosity values at a shear rate of at least 1000 second ⁇ 1 are of specific interest because these are the typical conditions found in commercial fiber spinning extruders.
  • a gas permeation chromatography (GPC) method is used to determine the molecular weight distribution of samples, such as of poly(lactic acid) whose weight average molecular weight (M w ) is between about 800 to about 400,000.
  • the GPC is set up with two PLgel Mixed K linear 5 micron, 7.5 ⁇ 300 millimeter analytical columns in series.
  • the column and detector temperatures are 30° C.
  • the mobile phase is high-performance liquid chromatography (HPLC) grade tetrahydrofuran (THF).
  • HPLC high-performance liquid chromatography
  • THF high-performance liquid chromatography
  • the pump rate is 0.8 milliliter per minute with an injection volume of 25 microliters. Total run time is 30 minutes. It is important to note that new analytical columns must be installed about every 4 months, a new guard column about every month, and a new in-line filter, about every month.
  • Standard 1 401,340; 32,660; 2,727
  • Standard 2 45,730; 4,075
  • Standard 3 95,800; 12,860
  • Standard 4 184,200; 24,150; 687).
  • Sample preparations begins by weighing 0.080 g ⁇ 0.0025 g of the sample into a clean, dry scintillation vial (great care should also be taken in its weighing and preparation). Add 2 ml of DCM to the vial with a volumetric pipet or dedicated repipet and screw the cap on tightly. Allow the sample to dissolve completely using the same technique described in the check standard preparation above. Then add 18 ml of THF using a volumetric pipet or dedicated repipet, cap the vial tightly and mix.
  • the correlation coefficient of the fourth order regression calculated for each standard should be not less than 0.950 and not more than 1.050.
  • the relative standard deviation of all the weight average molecular weights of the check standard preparations should not be more than 5.0 percent.
  • the average of the weight average molecular weights of the check standard preparation injections should be within 10 percent of the weight average molecular weight on the first check standard preparation injection.
  • the required equipment for the determination of heat shrinkage include: a convection oven (Thelco model 160DM laboratory oven, available from Precision and Scientific Inc., of Chicago, Ill.), 0.5 g (+/ ⁇ 0.06 g) sinker weights, 1 ⁇ 2 inch binder clips, masking tape, graph paper with at least 1 ⁇ 4 inch squares, foam posterboard (11 by 14 inches) or equivalent substrate to attach the graph paper and samples to.
  • the convection oven should be capable of a temperature of about 90° C.
  • Fiber samples are melt spun at their respective spinning conditions.
  • a 30 filament bundle is preferred and mechanically drawn to obtain fibers with a jetstretch ratio of beneficially 50 or higher. Only fibers of the same jetstretch ratio can be compared to one another in regards to their heat shrinkage.
  • the jetstretch ratio of a fiber is the ratio of the speed of the drawdown roll divided by the linear extrusion rate (distance/time) of the melted polymer exiting the spinneret.
  • the spun fiber is usually collected onto a bobbin using a winder. The collected fiber bundle is separated into 30 filaments, if a 30 filament bundle has not already been obtained, and cut into 9 inch lengths.
  • the graph paper is taped onto the posterboard where one edge of the graph paper is matched with the edge of the posterboard.
  • One end of the fiber bundle is taped, no more than the end 1 inch.
  • the taped end is clipped to the posterboard at the edge where the graph paper is matched up such that the edge of the clip rests over one of the horizontal lines on the graph paper while holding the fiber bundle in place (the taped end should be barely visible as it is secured under the clip).
  • the other end of the bundle is pulled taught and lined up parallel to the vertical lines on the graph paper.
  • pinch the 0.5 g sinker around the fiber bundle are then the attachment process for each replicate. Usually, 3 replicates can be attached at one time.
  • Marks can be made on the graph paper to indicate the initial positions of the sinkers.
  • the samples are placed into the oven at a temperature of about 90° C. such that the samples hang vertically and do not touch the posterboard.
  • time intervals of 5, 10 and 15 minutes quickly mark the new location of the sinkers on the graph paper and return samples to the oven.
  • the Heat Shrinkage value represents the amount of heat shrinkage that a fiber sample exhibits at a temperature of about 90° C for a time period of about 15 minutes, as determined according to the preceding test method.
  • the equipment includes a DCA-322 Dynamic Contact Angle Analyzer and WinDCA (version 1.02) software, both available from ATI-CAHN Instruments, Inc., of Madison, Wis. Testing was done on the “A” loop with a balance stirrup attached. Calibrations should be done monthly on the motor and daily on the balance (100 mg mass used) as indicated in the manual.
  • Thermoplastic compositions are spun into fibers and the freefall sample Oetstretch of 0) is used for the determination of contact angle. Care should be taken throughout fiber preparation to minimize fiber exposure to handling to ensure that contamination is kept to a minimum.
  • the fiber sample is attached to the wire hanger with scotch tape such that 2-3 cm of fiber extends beyond the end of the hanger. Then the fiber sample is cut with a razor so that 1.5 cm is extending beyond the end of the hanger. An optical microscope is used to determine the average diameter (3 to 4 measurements) along the fiber.
  • the sample on the wire hanger is suspended from the balance stirrup on loop “A”.
  • the immersion liquid is distilled water and it is changed for each specimen.
  • the specimen parameters are entered (i.e. fiber diameter) and the test started.
  • the stage advances at 151.75 microns/second until it detects the Zero Depth of Immersion when the fiber contacts the surface of the distilled water. From the Zero Depth of Immersion, the fiber advances into the water for 1 cm, dwells for 0 seconds and then immediately recedes 1 cm.
  • the auto-analysis of the contact angle done by the software determines the advancing and receding contact angles of the fiber sample based on standard calculations identified in the manual. Contact angles of 0 or ⁇ 0 indicate that the sample has become totally wettable.
  • the Advancing Contact Angle value represents the advancing contact angle of distilled water on a fiber sample determined according to the preceding test method.
  • the Receding Contact Angle value represents the receding contact angle of distilled water on a fiber sample determined according to the preceding test method.
  • a suitable technique for determining the mechanical properties of the fiber can employ a Sintech tensile tester (SINTECH 1/D) and Testworks 3.03 software, both available from MTS System Co., of Cary, N.C. Equipment and software having substantially equivalent capabilities may also be employed.
  • Fiber testing is carried out using a 10 pound load cell and fiber grips. It is necessary to have grips which are designated for the testing of fibers. Numerous configurations which fulfill this purpose are available from the aforementioned MTS System Co. All fiber testing is done using a one-inch gauge length and 500 mm/minute grip separation speed. A bundle of 30 fibers is threaded into the grips with care taken to minimize the chance for any contamination.
  • An extrapolated diameter for the fiber bundle is determined from the average diameter of the individual fibers determined via optical microscopy and converted into a theoretical diameter for the fiber bundle as if it were a single fiber.
  • the fiber bundle is stretched until breakage occurs and the software creates a stress-versus-strain plot and calculates the mechanical properties for the sample.
  • Mechanical properties of interest in the study are break stress and percent strain at the break. Five replicates are run and a statistical analysis performed.
  • the fiber is stretched untl breakage occurs and the software creates a stress-versus-strain plot and calculates the desired mechanical properties for the sample.
  • the mechanical properties can include, for example, Young's modulus, stress at break, and percent strain or elongation at break.
  • thermoplastic compositions and multicomponent fibers were used as components to form thermoplastic compositions and multicomponent fibers in the following Examples. The designation and various properties of these materials are listed in Table 1.
  • Samples 1 and 2 are poly(lactc acid) (PLA) polymers obtained from Chronopol Inc., Golden, Colo.
  • PBS polybutylene succinate
  • PBS polybutylene succinate
  • the wetting agent used throughout the examples was obtained from Petrolite Corporation of Tulsa, Okla., under the designation UNITHOX® 480 ethoxylated alcohol, which exhibited a number average molecular weight of about 2250, an ethoxylate percent of about 80 weight percent, and an HLB value of about 16.
  • Thermoplastic compositions were prepared using varying amounts of a poly(lactic acid) polymer, a polybutylene succinate, and a wetting agent.
  • a specific thermoplastic composition the various components were first dry mixed and then melt blended in a counter-rotating twin screw to provide vigorous mixing of the components.
  • the melt mixing involves partial or complete melting of the components combined with the shearing effect of rotating mixing screws. Such conditions are conducive to optimal blending and even dispersion of the components of the thermoplastic composition.
  • Twin screw extruders such as a Haake Rheocord 90, available from Haake GmbH of Karlsautte, Germany, or a Brabender twin screw mixer (cat no 05-96-000) available from Brabender Instruments of Southhackensack, N.J., or other comparable twin screw extruders, are well suited to this task.
  • the melted composition is cooled following extrusion from the melt mixer on either a liquid cooled roll or surface and/or by forced air passed over the extrudate.
  • the cooled composition is then subsequently pelletized for conversion to fibers.
  • each heating zone is indicated sequentially under the extrusion temperatures heading in Table 2.
  • the fibers are air quenched using air at a temperature range of 13° C. to 22° C., and drawn down by a mechanical draw roll and passed on to either a winder unit for collection, or to a fiber drawing unit for spunbond formation and bonding, or through accessory equipment for heat setting or other treatment before collection.
  • the fibers were then evaluated for contact angle and heat shrinkage.
  • the composition of the various fibers and the results of the evaluations are shown in Table 3.

Abstract

Disclosed is a thermoplastic composition comprising an unreacted mixture of a poly(lactic acid) polymer, a polybutylene succinate polymer or a polybutylene succinate adipate polymer, or a mixture of such polymers; and a wetting agent. The thermoplastic composition exhibits substantial biodegradable properties yet is easily processed. The thermoplastic composition is useful in making multicomponent fibers or nonwoven structures that may be used in a disposable absorbent product intended for the absorption of fluids such as body fluids.

Description

This application is a divisional of application Ser. No. 08/962,432 entitled BIODEGRADEABLE THERMOPLASTIC COMPOSITION and filed in the U.S. Patent and Trademark Office on Oct. 31, 1997 now U.S. Pat. No. 5,910,545. The entirety of application Ser. No. 08/962,432 is hereby incorporated by reference.
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a thermoplastic composition. The thermoplastic composition comprises an unreacted mixture of a poly(lactic acid) polymer, a polybutylene succinate polymer or a polybutylene succinate adipate polymer or a mixture of such polymers, and a wetting agent. The thermoplastic composition exhibits substantial biodegradable properties yet is easily processed. The thermoplastic composition is useful in making multicomponent fibers or nonwoven structures that may be used in a disposable absorbent product intended for the absorption of fluids such as body fluids.
2. Description of the Related Art
Disposable absorbent products currently find widespread use in many applications. For example, in the infant and child care areas, diapers and training pants have generally replaced reusable cloth absorbent articles. Other typical disposable absorbent products include feminine care products such as sanitary napkins or tampons, adult incontinence products, and health care products such as surgical drapes or wound dressings. A typical disposable absorbent product generally comprises a composite structure including a topsheet, a backsheet, and an absorbent structure between the topsheet and backsheet. These products usually include some type of fastening system for fitting the product onto the wearer.
Disposable absorbent products are typically subjected to one or more liquid insults, such as of water, urine, menses, or blood, during use. As such, the outer cover backsheet materials of the disposable absorbent products are typically made of liquid-insoluble and liquid impermeable materials, such as polypropylene films, that exhibit a sufficient strength and handling capability so that the disposable absorbent product retains its integrity during use by a wearer and does not allow leakage of the liquid insulting the product.
Although current disposable baby diapers and other disposable absorbent products have been generally accepted by the public, these products still have need of improvement in specific areas. For example, many disposable absorbent products can be difficult to dispose of. For example, attempts to flush many disposable absorbent products down a toilet into a sewage system typically lead to blockage of the toilet or pipes connecting the toilet to the sewage system. In particular, the outer cover materials typically used in the disposable absorbent products generally do not disintegrate or disperse when flushed down a toilet so that the disposable absorbent product cannot be disposed of in this way. If the outer cover materials are made very thin in order to reduce the overall bulk of the disposable absorbent product so as to reduce the likelihood of blockage of a toilet or a sewage pipe, then the outer cover material typically will not exhibit sufficient strength to prevent tearing or ripping as the outer cover material is subjected to the stresses of normal use by a wearer.
Furthermore, solid waste disposal is becoming an ever increasing concern throughout the world. As landfills continue to fill up, there has been an increased demand for material source reduction in disposable products, the incorporation of more recyclable and or degradable components in disposable products, and the design of products that can be disposed of by means other than by incorporation into solid waste disposal facilities such as landfills.
As such, there is a need for new materials that may be used in disposable absorbent products that generally retain their integrity and strength during use, but after such use, the materials may be more efficiently disposed of. For example, the disposable absorbent product may be easily and efficiently disposed of by composting. Alternatively, the disposable absorbent product may be easily and efficiently disposed of to a liquid sewage system wherein the disposable absorbent product is capable of being degraded.
Although degradable monocomponent fibers are known, problems have been encountered with their use. In particular, known degradable fibers typically do not have good thermal dimensional stability such that the fibers usually undergo severe heat-shrinkage due to the polymer chain relaxation during downstream heat treatment processes such as thermal bonding or lamination.
For example, although fibers prepared from poly(lactic acid) polymer are known, problems have been encountered with their use. In particular, poly(lactic acid) polymers are known to have a relatively slow crystallization rate as compared to, for example, polyolefin polymers, thereby often resulting in poor processability of the aliphatic polyester polymers. In addition, the poly(lactic acid) polymers generally do not have good thermal dimensional-stability. The poly(lactic acid) polymers usually undergo severe heat-shrinkage due to the relaxation of the polymer chain during downstream heat treatment processes, such as thermal bonding and lamination, unless an extra step such as heat setting is taken. However, such a heat setting step generally limits the use of the fiber in in-situ nonwoven forming processes, such as spunbond and meltblown, where heat setting is very difficult to be accomplished.
It is therefore an object of the present invention to provide a thermoplastic composition which exhibits desired processability, liquid wettability, and thermal dimensional-stability properties.
It is also an object of the present invention to provide a thermoplastic composition which may be easily and efficiently formed into a fiber.
It is also an object of the present invention to provide a thermoplastic composition which is suitable for use in preparing nonwoven structures.
It is also an object of the present invention to provide a fiber or nonwoven structure that is readily degradable in the environment.
It is also an object of the present invention to provide a disposable absorbent product that may be used for the absorption of fluids such as bodily fluids, yet which such disposable absorbent product comprises components that are readily degradable in the environment.
SUMMARY OF THE INVENTION
The present invention concerns a thermoplastic composition that is substantially biodegradable and yet which is easily prepared and readily processable into desired final structures, such as fibers or nonwoven structures.
One aspect of the present invention concerns a thermoplastic composition that comprises a mixture of a first component, a second component, and a third component.
One embodiment of such a thermoplastic composition comprises an unreacted mixture of a poly(lactic acid) polymer; a polybutylene succinate polymer or a polybutylene succinate adipate polymer or a mixture of such polymers; and a wetting agent for the poly(lactic acid) polymer, the polybutylene succinate polymer or the polybutylene succinate adipate polymer or a mixture of such polymers.
In another aspect, the present invention concerns a multicomponent fiber that is substantially degradable and yet which is easily prepared and readily processable into desired final structures, such nonwoven structures.
One aspect of the present invention concerns a multicomponent fiber that comprises an unreacted mixture of a poly(lactic acid) polymer; a polybutylene succinate polymer or a polybutylene succinate adipate polymer or a mixture of such polymers; and a wetting agent for the aliphatic polyester polymer and the polybutylene succinate polymer or the polybutylene succinate adipate polymer or a mixture of such polymers.
In another aspect, the present invention concerns a nonwoven structure comprising the multicomponent fiber disclosed herein.
One embodiment of such a nonwoven structure is a frontsheet useful in a disposable absorbent product.
In another aspect, the present invention concerns a process for preparing the multicomponent fiber disclosed herein.
In another aspect, the present invention concerns a disposable absorbent product comprising the multicomponent fiber disclosed herein.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
The present invention is directed to a thermoplastic composition which includes a first component, a second component, and a third component. As used herein, the term “thermoplastic” is meant to refer to a material that softens when exposed to heat and substantially returns to its original condition when cooled to room temperature.
It has been discovered that, by using an unreacted mixture of a poly(lactic acid) polymer, a polybutylene succinate polymer or a polybutylene succinate adipate polymer or a mixture of such polymers, and a wetting agent, a thermoplastic composition may be prepared wherein such thermoplastic composition is substantially degradable yet which thermoplastic composition is easily processed into fibers and nonwoven structures that exhjbit effective fibrous mechanical properties.
The first component in the thermoplastic composition is poly(lactic acid) polymer. Poly(lactic add) polymer is generally prepared by the polymerization of lactic acid. However, it will be recognized by one skilled in the art that a chemically equivalent material may also be prepared by the polymerization of lactide. As such, as used herein, the term “poly(lactic acid) polymer” is intended to represent the polymer that is prepared by either the polymerization of lactic acid or lactide.
Lactic acid and lactide are known to be asymmetrical molecules, having two optical isomers referred to, respectively, as the levorotatory (hereinafter referred to as “L”) enantiomer and the dextrorotatory (hereinafter referred to as “D”) enantiomer. As a result, by polymerizing a particular enantiomer or by using a mixture of the two enantiomers, it is possible to prepare different polymers that are chemically similar yet which have different properties. In particular, it has been found that by modifying the stereochemistry of a poly(lactic add) polymer, it is possible to control, for example, the melting temperature, melt rheology, and crystallinity of the polymer. By being able to control such properties, it is possible to prepare a thermoplastic composition and a multicomponent fiber exhibiting desired melt strength, mechanical properties, softness, and processability properties so as to be able to make attenuated, heat-set, and crimped fibers.
Examples of poly(lactic acid) polymers that are suitable for use in the present invention include a variety of poly(lactic acid) polymers that are available from Chronopol Inc., Golden, Colo.
It is generally desired that the poly(lactic acid) polymer be present in the thermoplastic composition in an amount effective to result in the thermoplastic composition exhibiting desired properties. The poly(lactic acid) polymer will be present in the thermoplastic composition in a weight amount that is greater than 0 but less than 100 weight percent, beneficially between about 5 weight percent to about 95 weight percent, suitably between about 10 weight percent to about 90 weight percent, and more suitably between about 15 weight percent to about 85 weight percent, wherein all weight percents are based on the total weight amount of the poly(lactic acid) polymer, the polybutylene succinate polymer or polybutylene succinate adipate polymer or a mixture of such polymers, and the wetting agent present in the thermoplastic composition. The compositional ratio of the three components in the thermoplastic composition is generally important to obtain the desired properties of the thermoplastic composition, such as wettability, biodegradability, thermal stability and processability.
The second component in the thermoplastic composition is a polybutylene succinate polymer, a polybutylene succinate adipate polymer, or a mixture of such polymers. A polybutylene succinate polymer is generally prepared by the condensation polymerization of a glycol and a dicarboxylic acid or an acid anhydride thereof. A polybutylene succinate polymer may either be a linear polymer or a long-chain branched polymer. A long-chain branched polybutylene succinate polymer is generally prepared by using an additional polyfunctional component selected from the group consisting of trifunctional or tetrafunctional polyols, oxycarboxylic acids, and polybasic carboxylic acids. Polybutylene succinate polymers are known in the art and are described, for example, in European Patent Application 0 569 153 A2 to Showa Highpolymer Co., Ltd., Tokyo, Japan. A polybutylene succinate adipate polymer is generally prepared by the polymerization of at least one alkyl glycol and more than one aliphatic multifunctional acid. Polybutylene succinate adipate polymers are also known in the art.
Examples of polybutylene succinate polymers and polybutylene succinate adipate polymers that are suitable for use in the present invention include a variety of polybutylene succinate polymers and polybutylene succinate adipate polymers that are available from Showa Highpolymer Co., Ltd., Tokyo, Japan, under the designation Bionolle 1903 polybutylene succinate polymer, with long chain branches, or Bionolle 1020 polybutylene succinate polymer, which is an essentially linear polymer.
It is generally desired that the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers be present in the thermoplastic composition in an amount effective to result in the thermoplastic composition exhibiting desired properties. The polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers will be present in the thermoplastic composition in a weight amount that is greater than 0 but less than 100 weight percent, beneficially between about 5 weight percent to about 95 weight percent, suitably between about 10 weight percent to about 90 weight percent, and more suitably between about 15 weight percent to about 85 weight percent, wherein all weight percents are based on the total weight amount of The poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent present in the thermoplastic composition.
It is generally desired that the poly(lactic acid) polymer and the polybutylene succinate polymer and/or the polybutylene succinate adipate polymer exhibit a weight average molecular weight that is effective for the thermoplastic composition to exhibit desirable melt strength, fiber mechanical strength, and fiber spinning properties. In general, if the weight average molecular weight of a particular polymer is too high, this represents that the polymer chains are heavily entangled which may result in a thermoplastic composition comprising that polymer being difficult to process. Conversely, if the weight average molecular weight of a particular polymer is too low, this represents that the polymer chains are not entangled enough which may result in a thermoplastic composition comprising that polymer exhibiting a relatively weak melt strength, making high speed processing very difficult. Thus, poly(lactic acid) polymers, polybutylene succinate polymers, and/or polybutylene succinate adipate polymers suitable for use in the present invention respectively exhibit weight average molecular weights that are beneficially between about 10,000 to about 2,000,000, more beneficially between about 50,000 to about 400,000, and suitably between about 100,000 to about 300,000. The weight average molecular weight for polymers or polymer blends can be determined using a method as described in the Test Methods section herein.
It is also desired that the poly(lactic acid) polymer and the polybutylene succinate polymer and/or the polybutylene succinate adipate polymer exhibit a polydispersity index value that is effective for the thermoplastic composition to exhibit desirable melt strength, fiber mechanical strength, and fiber spinning properties. As used herein, “polydispersity index” is meant to represent the value obtained by dividing the weight average molecular weight of a polymer by the number average molecular weight of the polymer. In general, if the polydispersity index value of a particular polymer is too high, a thermoplastic composition comprising that polymer may be difficult to process due to inconsistent processing properties caused by polymer segments comprising low molecular weight polymers that have lower melt strength properties during spinning. Thus, it is desired that the poly(lactic acid) polymer, the polybutylene succinate polymer, and/or the polybutylene succinate adipate polymer respectively exhibit a polydispersity index value that is beneficially between about 1 to about 15, more beneficially between about 1 to about 4, and suitably between about 1 to about 3. The number average molecular weight for polymers or polymer blends can be determined using a method as described in the Test Methods section herein.
In the present invention, it is desired that the poly(lactic acid) polymer, the olybutylene succinate polymer, and the polybutylene succinate adipate polymer be biodegradable. As a result, the thermoplastic composition comprising these polymers, either in the form of a fiber or in the form of a nonwoven structure, will be substantially degradable when disposed of to the environment and exposed to air and/or water. As used herein, “biodegradable” is meant to represent that a material degrades from the action of naturally occurring microorganisms such as bacteria, fungi, and algae.
In the present invention, it is also desired that the poly(lactic acid) polymer, the polybutylene succinate polymer, and the polybutylene succinate adipate polymer be compostable. As a result, the thermoplastic composition comprising these polymers, either in the form of a fiber or in the form of a nonwoven structure, will be substantially compostable when disposed of to the environment and exposed to air and/or water. As used herein, “compostable” is meant to represent that a material is capable of undergoing biological decomposition in a compost site such that the material is not visually distinguishable and breaks down into carbon dioxide, water, inorganic compounds, and biomass, at a rate consistent with known compostable materials.
As used herein, the term “hydrophobic” refers to a material having a contact angle of water in air of at least 90 degrees. In contrast, as used herein, the term “hydrophilic” refers to a material having a contact angle of water in air of less than 90 degrees. For the purposes of this application, contact angle measurements are determined as set forth in the Test Methods section herein. The general subject of contact angles and the measurement thereof is well known in the art as, for example, in Robert J. Good and Robert J. Stromberg, Ed., in “Surface and Colloid Science—Experimental Methods”, Vol. 11, (Plenum Press, 1979).
It is generally desired that the poly(lactic acid) polymer, the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers, be melt processable. It is therefore desired that the polymers used in the present invention exhibit a melt flow rate that is beneficially between about 1 gram per 10 minutes to about 600 grams per 10 minutes, suitably between about 5 grams per 10 minutes to about 200 grams per 10 minutes, and more suitably between about 10 grams per 10 minutes to about 150 grams per 10 minutes. The melt flow rate of a material may be determined according to ASTM Test Method D1238-E, incorporated in its entirety herein by reference.
As used herein, the term “fiber” or “fibrous” is meant to refer to a material wherein the length to diameter ratio of such material is greater than about 10. Conversely, a “nonfiber” or “nonfibrous” material is meant to refer to a material wherein the length to diameter ratio of such material is about 10 or less.
Either separately or when mixed together, the poly(lactic acid) polymer and the polybutylene succinate polymer and/or the polybutylene succinate adipate polymer are generally hydrophobic. Since it is desired that the thermoplastic composition of the present invention, and fibers prepared from the thermoplastic composition, generally be hydrophilic, it has been found that there is a need for the use of another component in the thermoplastic composition of the present invention in order to achieve the desired properties. Furthermore, it has been found desirable to improve the processability of the poly(lactic acid) polymer, and the polybutylene succinate polymer and/or the polybutylene succinate adipate, since such polymers are not chemically identical and are, therefore, somewhat incompatible with each other which negatively affects the processing of a mixture of such polymers. For example, the poly(lactic acid) polymer, the polybutylene succinate polymer, and/or the polybutylene succinate adipate polymer are sometimes difficult to effectively mix and prepare as an essentially homogeneous mixture on their own. As such, the present invention generally requires the use of a wetting agent that allows for the effective preparation and processing of the poly(lactic acid) polymer, the polybutylene succinate polymer, and/or the polybutylene succinate adipate polymer into a single thermoplastic composition.
Thus, the third component in the thermoplastic composition is a wetting agent for the poly(lactic acid) polymer and the polybutylene succinate polymer and/or the polybutylene succinate adipate polymer. Wetting agents suitable for use in the present invention will generally comprise a hydrophilic section which will generally be compatible to poly(lactic acid) polymer and the hydrophilic sections of polybutylene succinate polymer or polybutylene succinate adipate polymer and a hydrophobic section which will generally be compatible to the hydrophobic sections of polybutylene succinate polymer or polybutylene succinate adipate polymer. These hydrophilic and hydrophobic sections of the wetting agent will generally exist in separate blocks so that the overall wetting agent structure may be di-block or random block. It is generally desired that the wetting agent initially functions as a plasticizer and an agent to enhance cohesion between the different polymers in order to improve the preparation and processing of the thermoplastic composition. It is then generally desired that the wetting agent then serves as a surfactant in a material processed from the thermoplastic composition, such as a fiber or nonwoven structure, by modifying the contact angle of water in air of the processed material. The hydrophobic portion of the wetting agent may be, but is not limited to, a polyolefin such as polyethylene or polypropylene. The hydrophilic portion of the wetting agent may contain ethylene oxide, ethoxylates, glycols, alcohols or any combinations thereof. Examples of suitable wetting agents include UNITHOX® 480 and UNITHOX® 0750 ethoxylated alcohols, or UNICID® Acid Amide Ethoxylates, all available from Petrolite Corporation of Tulsa, Okla.
It is generally desired that the wetting agent exhibit a weight average molecular weight that is effective for the thermoplastic composition to exhibit desirable melt strength, fiber mechanical strength, and fiber spinning properties. In general, if the weight average molecular weight of a wetting agent is too high, the wetting agent will not blend well with the other components in the thermoplastic composition because the wetting agent's viscosity will be so high that it lacks the mobility needed to blend. Conversely, if the weight average molecular weight of the wetting agent is too low, this represents that the wetting agent will generally not blend well with the other components and have such a low viscosity that it causes processing problems. Thus, wetting agents suitable for use in the present invention exhibit weight average molecular weights that are beneficially between about 1,000 to about 100,000, suitably between about 1,000 to about 50,000, and more suitably between about 1,000 to about 10,000. The weight average molecular weight for a material can be determined using a method as described in the Test Methods section herein.
It is generally desired that the wetting agent exhibit an effective hydrophilic-lipophilic balance ratio (HLB ratio). The HLB ratio of a material describes the relative ratio of the hydrophilicity of the material. The HLB ratio is calculated as the weight average molecular weight of the hydrophilic portion divided by the total weight average molecular weight of the material, which value is then multiplied by 20. If the HLB ratio value is too low, the wetting agent will generally not provide the desired improvement in hydrophilicity. Conversely, if the HLB ratio value is too high, the wetting agent will not blend into the thermoplastic composition because of chemical incompatibility and differences in viscosities with the other components. Thus, wetting agents useful in the present invention exhibit HLB ratio values that are beneficially between about 10 to about 40, suitably between about 10 to about 20, and more suitably between about 12 to about 16.
It is generally desired that the wetting agent be present in the thermoplastic composition in an amount effective to result in the thermoplastic composition exhibiting desired properties such as desirable heat shrinkage and desirable contact angle values. In general, a minimal amount of the wetting agent will be needed to achieve an effective blending and processing with the other components in the thermoplastic composition. In general, too much of the compatibilizer may lead to processing problems of the thermoplastic composition or to a final thermoplastic composition that does not exhibit desired properties such as desired advancing and receding contact angle values. The wetting agent will be present in the thermoplastic composition in a weight amount that is greater than 0 to about 15 weight percent, beneficially between about 0.5 weight percent to about 15 weight percent, more beneficially between about I weight percent to about 13 weight percent, suitably between about 1 weight percent to about 10 weight percent, and more suitably between about 1 weight percent to about 5 weight percent, wherein all weight percents are based on the total weight amount of the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent present in the thermoplastic composition.
While the principal components of the thermoplastic composition of the present invention have been described in the foregoing, such thermoplastic composition is not limited thereto and can include other components not adversely effecting the desired properties of the thermoplastic composition. Exemplary materials which could be used as additional components would include, without limitation, pigments, antioxidants, stabilizers, surfactants, waxes, flow promoters, solid solvents, plasticizers, nucleating agents, particulates, and other materials added to enhance the processability of the thermoplastic composition. If such additional components are included in a thermoplastic composition, it is generally desired that such additional components be used in an amount that is beneficially less than about 10 weight percent, more beneficially less than about 5 weight percent, and suitably less than about 1 weight percent, wherein all weight percents are based on the total weight amount of the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent present in the thermoplastic composition.
The thermoplastic composition of the present invention is generally simply a mixture of the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; the wetting agent, and, optionally, any additional components. In order to achieve the desired properties for the thermoplastic composition of the present invention, it is desirable that the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent remain substantially unreacted with each other. As such, each of the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent remain distinct components of the thermoplastic composition.
Each of the poly(lactic acid) polymer and the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers will generally form separate regions or domains within a prepared mixture forming the thermoplastic composition. However, depending on the relative amounts that are used of each of the poly(lactic acid) polymer and the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers, an essentially continuous phase may be formed from the polymer that is present in the thermoplastic composition in a relatively greater amount. In contrast, the polymer that is present in the thermoplastic composition in a relatively lesser amount may form an essentially discontinuous phase, forming separate regions or domains within the continuous phase of the more prevalent polymer wherein the more prevalent polymer continuous phase substantially encases the less prevalent polymer within its structure. As used herein, the term “encase”, and related terms, are intended to mean that the more prevalent polymer continuous phase substantially encloses or surrounds the less prevalent polymer's separate regions or domains.
In one embodiment of a thermoplastic composition or a multicomponent fiber of the present invention, it is desired that the poly(lactic acid) polymer form an essentially continuous phase and that the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers form an essentially discontinuous phase, wherein the poly(lactic acid) polymer substantially encases regions or domains of the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers. In such an embodiment, it is desired that the poly(lactic acid) polymer is present in the thermoplastic composition or multicomponent fiber in a weight amount that is between about 75 weight percent to about 90 weight percent and that the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers is present in the thermoplastic composition or multicomponent fiber in a weight amount that is between about 5 weight percent to about 20 weight percent, wherein all weight percents are based on the total weight amount of the poly(lactic acid) polymer, the polybutylene succinate polymer or polybutylene succinate adipate polymer or a mixture of such polymers, and the wetting agent present in the thermoplastic composition or the multicomponent fiber.
In one embodiment of the present invention, after dry mixing together the poly(lactic acid) polymer; the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent to form a thermoplastic composition dry mixture, such thermoplastic composition dry mixture is beneficially agitated, stirred, or otherwise blended to effectively uniformly mix the poly(lactic acid) polymer, the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent such that an essentially homogeneous dry mixture is formed. The dry mixture may then be melt blended in, for example, an extruder, to effectively uniformly mix the poly(lactic acid) polymer, the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers; and the wetting agent such that an essentially homogeneous melted mixture is formed. The essentially homogeneous melted mixture may then be cooled and pelletized. Altematively, the essentially homogeneous melted mixture may be sent directly to a spin pack or other equipment for forming fibers or a nonwoven structure.
Alternative methods of mixing together the components of the present invention include first mixing together the poly(lactic acid) polymer and the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers and then adding the wetting agent to such a mixture in, for example, an extruder being used to mix the components together. In addition, it is also possible to initially melt mix all of the components together at the same time. Other methods of mixing together the components of the present invention are also possible and will be easily recognized by one skilled in the art.
The present invention is also directed to a multicomponent fiber which is prepared from the thermoplastic composition of the present invention. For purposes of illustration only, the present invention will generally be described in terms of a multicomponent fiber comprising only three components. However, it should be understood that the scope of the present invention is meant to include fibers with three or more components.
When the thermoplastic composition of the present invention is formed into a multicomponent fiber, an exposed surface on at least a portion of the multicomponent fiber will typically be formed from the more prevalent polymer present in the multicomponent fiber. Such an exposed surface on at least a portion of the multicomponent fiber which will generally permit thermal bonding of the multicomponent fiber to other fibers which may be the same or different from the multicomponent fiber of the present invention. As a result, the multicomponent fiber can then be used to form thermally bonded fibrous nonwoven structures such as a nonwoven web.
Typical conditions for thermally processing the various components indude using a shear rate that is beneficially between about 100 seconds−1 to about 50000 seconds−1, more beneficially between about 500 seconds−1 to about 5000 seconds−1, suitably between about 1000 seconds−1 to about 3000 seconds−1, and most suitably at about 1000 seconds−1. Typical conditions for thermally processing the components also include using a temperature that is beneficially between about 100° C. to about 500° C., more beneficially between about 150° C. to about 300 °C, and suitably between about 175° C. to about 250° C.
Methods for making multicomponent fibers are well known and need not be described here in detail. The melt spinning of polymers includes the production of continuous filament, such as spunbond or meltblown, and non-continuous filament, such as staple and shortcut fibers. To form a spunbond or meltblown fiber, generally, a thermoplastic composition is extruded and fed to a distribution system where the thermoplastic composition is introduced into a spinneret plate. The spun fiber is then cooled, solidified, and drawn by an aerodynamic system, to be formed into a conventional nonwoven. Meanwhile, to produce short-cut or staple fiber rather than being directly formed into a nonwoven structure the spun fiber is cooled, solidified, and drawn, generally by a mechanical rolls system, to an intermediate filament diameter and collected. Subsequently, the fiber may be “cold drawn” at a temperature below its softening temperature, to the desired finished fiber diameter and crimped or texturized and cut into a desirable fiber length.
Multicomponent fibers can be cut into relatively short lengths, such as staple fibers which generally have lengths in the range of about 25 to about 50 millimeters and short-cut fibers which are even shorter and generally have lengths less than about 18 millimeters.
The resultant multicomponent fibers of the present invention are desired to exhibit an improvement in hydrophilicity, evidenced by a decrease in the contact angle of water in air. The contact angle of water in air of a fiber sample can be measured as either an advancing or a receding contact angle value because of the nature of the testing procedure. The advancing contact angle measures a material's initial response to a liquid, such as water. The receding contact angle gives a measure of how a material will perform over the duration of a first insult, or exposure to liquid, as well as over following insults. A lower receding contact angle means that the material is becoming more hydrophilic during the liquid exposure and will generally then be able to transport liquids more consistently. Both the advancing and receding contact angle data is desirably used to establish the highly hydrophilic nature of a multicomponent fiber of the present invention.
In one embodiment of the present invention, it is desired that the multicomponent fiber exhibits an Advancing Contact Angle value that is beneficially less than about 80 degrees, more beneficially less than about 75 degrees, suitably less than about 70 degrees, more suitably less than about 60 degrees, and most suitably less than about 50 degrees, wherein the Advancing Contact Angle value is determined by the method that is described in the Test Methods section herein.
In another embodiment of the present invention, it is desired that the multicomponent fiber exhibits a Receding Contact Angle value that is beneficially less than about 60 degrees, more beneficially less than about 55 degrees, suitably less than about 50 degrees, more suitably less than about 45 degrees, and most suitably less than about 40 degrees, wherein the Receding Contact Angle value is determined by the method that is described in the Test Methods section herein.
In another embodiment of the present invention, it is desired that the difference between the Advancing Contact Angle value and the Receding Contact Angle value, commonly known as the contact angle hysteresis, be as small as possible. As such, it is desired that the multicomponent fiber exhibits a difference between the Advancing Contact Angle value and the Receding Contact Angle value that is beneficially less than about 30 degrees, more beneficially less than about 25 degrees, suitably less than about 20 degrees, and more suitably less than about 10 degrees.
Typical poly(lactic acid) polymer materials often undergo heat shrinkage during downstream thermal processing. The heat-shrinkage mainly occurs due to the thermally-induced chain relaxation of the polymer segments in the amorphous phase and incomplete crystalline phase. To overcome this problem, it is generally desirable to maximize the crystallization of the poly(lactic acid) polymer material before the bonding stage so that the thermal energy goes directly to melting rather than to allow for chain relaxation and reordering of the incomplete crystalline structure. The typical solution to this problem is to subject the material to a heat-setting treatment. As such, when prepared materials, such as fibers, are subjected to heat-setting upon reaching a bonding roll, the fibers won't substantially shrink because such fibers are already fully or highly oriented. The present invention alleviates the need for this additional processing step because of the composition of the multicomponent fiber of the present invention. In general, the addition of the polybutylene succinate polymer, the polybutylene succinate adipate polymer, or a mixture of such polymers, and the wetting agent decrease the heat shrinkage of a multicomponent fiber as compared to a fiber that is prepared from only poly(lactic acid) polymer.
In one embodiment of the present invention, it is desired that the multicomponent fiber exhibit an amount of shrinking, at a temperature of about 90° C., that is beneficially less than about 15 percent, more beneficially less than about 10 percent, and suitably less than about 5 percent, wherein the amount of shrinking is based upon the difference between the initial and final lengths of the fiber divided by the initial length of the fiber multiplied by 100. The method by which the amount of shrinking that a fiber exhibits may be determined is included in the Test Methods section herein.
In one embodiment of the present invention, it is desired that the multicomponent fiber exhibit an amount of shrinking, suitably less than about 5 percent at a temperature of about 90° C., that results in a nonwoven structure formed from the multicomponent fiber to exhibit a quilting or waviness effect that increases the surface area of the nonwoven structure since the shrinking of the multicomponent fibers causes the nonwoven structure to exhibit a three dimensional topography. Such a quilting or waviness effect of the nonwoven structure has been found to improve the softness and z-directional transport of a liquid within the nonwoven structure.
It is generally desired that multicomponent fibers also exhibit desired mechanical strength properties, such as a break stress value as well as a modulus value, such that the multicomponent fibers maintain their integrity during use. In one embodiment of the present invention, it is desired that a multicomponent fiber prepared from the thermoplastic composition of the present invention exhibits an improved break stress value as well as an improved modulus value as compared to a fiber that is prepared solely from poly(lactic acid) polymer. In one embodiment of the present invention, it is desired that a multicomponent fiber prepared from the thermoplastic composition of the present invention exhibits a break stress value that is at least twice the break stress value exhibited by an otherwise identical fiber that is prepared solely from the poly(lactic acid) polymer used to prepare the multicomponent fiber.
In one embodiment of the present invention, it is desired that the multicomponent fiber exhibit a break stress value that is greater than about 10 MPa, beneficially greater than about 15 MPa, suitably greater than about 20 MPa, and up to about 100 MPa.
In another embodiment of the present invention, it is desired that the multicomponent fiber exhibit a modulus value that is less than about 150 MPa, beneficially less than about 125 MPa, and suitably less than about 100 MPa.
The multicomponent fibers of the present invention are suited for use in disposable products including disposable absorbent products such as diapers, adult incontinent products, and bed pads; in catamenial devices such as sanitary napkins, and tampons; and other absorbent products such as wipes, bibs, wound dressings, and surgical capes or drapes. Accordingly, in another aspect, the present invention relates to a disposable absorbent product comprising the multicomponent fibers of the present invention.
In one embodiment of the present invention, the multicomponent fibers are formed into a fibrous matrix for incorporation into a disposable absorbent product. A fibrous matrix may take the form of, for example, a fibrous nonwoven web. Fibrous nonwoven webs may be made completely from the multicomponent fibers of the present invention or they may be blended with other fibers. The length of the fibers used may depend on the particular end use contemplated. Where the fibers are to be degraded in water as, for example, in a toilet, it is advantageous if the lengths are maintained at or below about 15 millimeters.
In one embodiment of the present invention, a disposable absorbent product is provided, which disposable absorbent product comprises a liquid-permeable topsheet, a backsheet attached to the liquid-permeable topsheet, and an absorbent structure positioned between the liquid-permeable topsheet and the backsheet, wherein the liquid-permeable topsheet comprises multicomponent fibers of the present invention.
Absorbent products and structures according to all aspects of the present invention are generally subjected, during use, to multiple insults of a body liquid. Accordingly, the absorbent products and structures are desirably capable of absorbing multiple insults of body liquids in quantities to which the absorbent products and structures will be exposed during use. The insults are generally separated from one another by a period of time.
TEST METHODS Melting Temperature
The melting temperature of a material was determined using differential scanning calorimetry. A differential scanning calorimeter, under the designation Thermal Analyst 2910 Differential Scanning Calorimeter, which was outfitted with a liquid nitrogen cooling accessory and used in combination with Thermal Analyst 2200 analysis software (version 8.10) program, both available from T.A. Instruments Inc. of New Castle, Del., was used for the determination of melting temperatures.
The material samples tested were either in the form of fibers or resin pellets. It is preferred to not handle the material samples directly, but rather to use tweezers and other tools, so as not to introduce anything that would produce erroneous results. The material samples were cut, in the case of fibers, or placed, in the case of resin pellets, into an aluminum pan and weighed to an accuracy of 0.01 mg on an analytical balance. If needed, a lid was crimped over the material sample onto the pan.
The differential scanning calorimeter was calibrated using an indium metal standard and a baseline correction performed, as described in the manual for the differential scanning calorimeter. A material sample was placed into the test chamber of the differential scanning calorimeter for testing and an empty pan is used as a reference. All testing was run with a 55 cubic centimeter/minute nitrogen (industrial grade) purge on the test chamber. The heating and cooling program is a 2 cycle test that begins with equilibration of the chamber to −75° C., followed by a heating cycle of 20° C./minute to 220° C., followed by a cooling cycle at 20° C./minute to −75° C., and then another heating cyde of 20° C./minute to 220° C.
The results were evaluated using the analysis software program wherein the glass transition temperature (Tg) of inflection, endothermic and exothermic peaks were identified and quantified. The glass transition temperature was identified as the area on the line where a distinct change in slope occurs and then the melting temperature is determined using an automatic inflection calculation.
Apparent Viscosity
A capillary rheometer, under the designation Göttfert Rheograph 2003 capillary rheometer, which was used in combination with WinRHEO (version 2.31) analysis software, both available from Göttfert Company of Rock Hill, S.C., was used to evaluate the apparent viscosity rheological properties of material samples. The capillary rheometer setup included a 2000 bar pressure transducer and a 30 mm length/30 mm active length/1 mm diameter/0 mm height180° run in angle, round hole capillary die.
If the material sample being tested demonstrates or is known to have water sensitivity, the material sample is dried in a vacuum oven above its glass transition temperature, i.e. above 55 or 60° C. for poly(lactic acid) materials, under a vacuum of at least 15 inches of mercury with a nitrogen gas purge of at least 30 standard cubic feet per hour for at least 16 hours.
Once the instrument is warmed up and the pressure transducer is calibrated, the material sample is loaded incrementally into the column, packing resin into the column with a ramrod each time to ensure a consistent melt during testing. After material sample loading, a 2 minute melt time precedes each test to allow the material sample to completely melt at the test temperature. The capillary rheometer takes data points automatically and determines the apparent viscosity (in Pascal. second) at 7 apparent shear rates (in second−1): 50, 100, 200, 500, 1000, 2000, and 5000. When examining the resultant curve it is important that the curve be relatively smooth. If there are significant deviations from a general curve from one point to another, possibly due to air in the column, the test run should be repeated to confirm the results.
The resultant rheology curve of apparent shear rate versus apparent viscosity gives an indication of how the material sample will run at that temperature in an extrusion process. The apparent viscosity values at a shear rate of at least 1000 second−1 are of specific interest because these are the typical conditions found in commercial fiber spinning extruders.
Molecular Weight
A gas permeation chromatography (GPC) method is used to determine the molecular weight distribution of samples, such as of poly(lactic acid) whose weight average molecular weight (Mw) is between about 800 to about 400,000.
The GPC is set up with two PLgel Mixed K linear 5 micron, 7.5×300 millimeter analytical columns in series. The column and detector temperatures are 30° C. The mobile phase is high-performance liquid chromatography (HPLC) grade tetrahydrofuran (THF). The pump rate is 0.8 milliliter per minute with an injection volume of 25 microliters. Total run time is 30 minutes. It is important to note that new analytical columns must be installed about every 4 months, a new guard column about every month, and a new in-line filter, about every month.
Standards of polystyrene polymers, obtained from Aldrich Chemical Co., should be mixed into a solvent of dichloromethane(DCM):THF (10:90), both HPLC grade, in order to obtain 1 mg/mL concentrations. Multiple polystyrene standards can be combined in one standard solution provided that their peaks do not overlap when chromatographed. A range of standards of about 687 to 400,000 molecular weight should be prepared. Examples of standard mixtures with Aldrich polystyrenes of varying weight average molecular weights include: Standard 1 (401,340; 32,660; 2,727), Standard 2 (45,730; 4,075), Standard 3 (95,800; 12,860) and Standard 4 (184,200; 24,150; 687).
Next, prepare the stock check standard. Dissolve 10 g of a 200,000 molecular weight poly(lactic acid) standard, Catalog#19245 obtained from Polysciences Inc., to 100ml of HPLC grade DCM to a glass jar with a lined lid using an orbital shaker (at least 30 minutes). Pour out the mixture onto a clean, dry, glass plate and first allow the solvent to evaporate, then place in a 35° C. preheated vacuum oven and dry for about 14 hours under a vacuum of 25 mm of mercury. Next, remove the poly(lactic acid) from the oven and cut the film into small strips. Immediately grind the samples using a grinding mill (with a 10 mesh screen) taking care not to add too much sample and causing the grinder to freeze up. Store a few grams of the ground sample in a dry glass jar in a dessicator, while the remainder of the sample can be stored in the freezer in a similar type jar.
It is important to prepare a new check standard prior to the beginning of each new sequence and, because the molecular weight is greatly affected by sample concentration, great care should be taken in its weighing and preparation. To prepare the check standard weigh out 0.0800 g ±0.0025 g of 200,000 weight average molecular weight poly(lactic acid) reference standard into a clean dry scintillation vial. Then, using a volumetric pipet or dedicated repipet, add 2 ml of DCM to the vial and screw the cap on tightly. Allow the sample to dissolve completely. Swirl the sample on an orbital shaker, such as a Thermolyne Roto Mix (type 51300) or similar mixer, if necessary. To evaluate whether is it dissolved hold the vial up to the light at a 45° angle. Tum it slowly and watch the liquid as it flows down the glass. If the bottom of the vial does not appear smooth, the sample is not completely dissolved. It may take the sample several hours to dissolve. Once dissolved, add 18 ml of THF using a volumetric pipet or dedicated repipet, cap the vial tightly and mix.
Sample preparations begins by weighing 0.080 g ±0.0025 g of the sample into a clean, dry scintillation vial (great care should also be taken in its weighing and preparation). Add 2 ml of DCM to the vial with a volumetric pipet or dedicated repipet and screw the cap on tightly. Allow the sample to dissolve completely using the same technique described in the check standard preparation above. Then add 18 ml of THF using a volumetric pipet or dedicated repipet, cap the vial tightly and mix.
Begin the evaluation by making a test injection of a standard preparation to test the system equilibration. Once equilibration is confirmed inject the standard preparations. After those are run, first inject the check standard preparation and then the sample preparations. Inject the check standard preparation after every 7 sample injections and at the end of testing. Be sure not to take any more than two injections from any one vial, and those two injections must be made within 4.5 hours of each other.
There are 4 quality control parameters to assess the results. First, the correlation coefficient of the fourth order regression calculated for each standard should be not less than 0.950 and not more than 1.050. Second, the relative standard deviation of all the weight average molecular weights of the check standard preparations should not be more than 5.0 percent. Third, the average of the weight average molecular weights of the check standard preparation injections should be within 10 percent of the weight average molecular weight on the first check standard preparation injection. Lastly, record the lactide response for the 200 microgram per milliliter (μg/mL) standard injection on a SQC data chart. Using the chart's control lines, the response must be within the defined SQC parameters.
Calculate the Molecular statistics based on the calibration curve generated from the polystyrene standard preparations and constants for poly(lactic acid) and polystyrene in THF at 30° C. Those are: Polystyrene (K=14.1*105, alpha=0.700) and poly(lactic acid) (K=54.9*105, alpha=0.639).
Heat Shrinkage of Fibers
The required equipment for the determination of heat shrinkage include: a convection oven (Thelco model 160DM laboratory oven, available from Precision and Scientific Inc., of Chicago, Ill.), 0.5 g (+/−0.06 g) sinker weights, ½ inch binder clips, masking tape, graph paper with at least ¼ inch squares, foam posterboard (11 by 14 inches) or equivalent substrate to attach the graph paper and samples to. The convection oven should be capable of a temperature of about 90° C.
Fiber samples are melt spun at their respective spinning conditions. In general, a 30 filament bundle is preferred and mechanically drawn to obtain fibers with a jetstretch ratio of beneficially 50 or higher. Only fibers of the same jetstretch ratio can be compared to one another in regards to their heat shrinkage. The jetstretch ratio of a fiber is the ratio of the speed of the drawdown roll divided by the linear extrusion rate (distance/time) of the melted polymer exiting the spinneret. The spun fiber is usually collected onto a bobbin using a winder. The collected fiber bundle is separated into 30 filaments, if a 30 filament bundle has not already been obtained, and cut into 9 inch lengths.
The graph paper is taped onto the posterboard where one edge of the graph paper is matched with the edge of the posterboard. One end of the fiber bundle is taped, no more than the end 1 inch. The taped end is clipped to the posterboard at the edge where the graph paper is matched up such that the edge of the clip rests over one of the horizontal lines on the graph paper while holding the fiber bundle in place (the taped end should be barely visible as it is secured under the clip). The other end of the bundle is pulled taught and lined up parallel to the vertical lines on the graph paper. Next, at 7 inches down from the point where the clip is binding the fiber, pinch the 0.5 g sinker around the fiber bundle. Repeat the attachment process for each replicate. Usually, 3 replicates can be attached at one time. Marks can be made on the graph paper to indicate the initial positions of the sinkers. The samples are placed into the oven at a temperature of about 90° C. such that the samples hang vertically and do not touch the posterboard. At time intervals of 5, 10 and 15 minutes quickly mark the new location of the sinkers on the graph paper and return samples to the oven.
After the testing is complete, remove the posterboard and measure the distances between the origin (where the dip held the fibers) and the marks at 5, 10 and 15 minutes with a ruler graduated to {fraction (1/16)} inch. Three replicates per sample is recommended. Calculate averages, standard deviations and percent shrinkage. The percent shrinkage is calculated as (initial length—measured length) divided by the initial length and multiplied by 100. As reported in the examples herein and as used throughout the claims, the Heat Shrinkage value represents the amount of heat shrinkage that a fiber sample exhibits at a temperature of about 90° C for a time period of about 15 minutes, as determined according to the preceding test method.
Contact Angle
The equipment includes a DCA-322 Dynamic Contact Angle Analyzer and WinDCA (version 1.02) software, both available from ATI-CAHN Instruments, Inc., of Madison, Wis. Testing was done on the “A” loop with a balance stirrup attached. Calibrations should be done monthly on the motor and daily on the balance (100 mg mass used) as indicated in the manual.
Thermoplastic compositions are spun into fibers and the freefall sample Oetstretch of 0) is used for the determination of contact angle. Care should be taken throughout fiber preparation to minimize fiber exposure to handling to ensure that contamination is kept to a minimum. The fiber sample is attached to the wire hanger with scotch tape such that 2-3 cm of fiber extends beyond the end of the hanger. Then the fiber sample is cut with a razor so that 1.5 cm is extending beyond the end of the hanger. An optical microscope is used to determine the average diameter (3 to 4 measurements) along the fiber.
The sample on the wire hanger is suspended from the balance stirrup on loop “A”. The immersion liquid is distilled water and it is changed for each specimen. The specimen parameters are entered (i.e. fiber diameter) and the test started. The stage advances at 151.75 microns/second until it detects the Zero Depth of Immersion when the fiber contacts the surface of the distilled water. From the Zero Depth of Immersion, the fiber advances into the water for 1 cm, dwells for 0 seconds and then immediately recedes 1 cm. The auto-analysis of the contact angle done by the software determines the advancing and receding contact angles of the fiber sample based on standard calculations identified in the manual. Contact angles of 0 or <0 indicate that the sample has become totally wettable. Five replicates for each sample are tested and a statistical analysis for mean, standard deviation, and coefficient of variation percent are calculated. As reported in the examples herein and as used throughout the claims, the Advancing Contact Angle value represents the advancing contact angle of distilled water on a fiber sample determined according to the preceding test method. Similarly, as reported in the examples herein and as used throughout the claims, the Receding Contact Angle value represents the receding contact angle of distilled water on a fiber sample determined according to the preceding test method.
Mechanical ProDerties
A suitable technique for determining the mechanical properties of the fiber can employ a Sintech tensile tester (SINTECH 1/D) and Testworks 3.03 software, both available from MTS System Co., of Cary, N.C. Equipment and software having substantially equivalent capabilities may also be employed. Fiber testing is carried out using a 10 pound load cell and fiber grips. It is necessary to have grips which are designated for the testing of fibers. Numerous configurations which fulfill this purpose are available from the aforementioned MTS System Co. All fiber testing is done using a one-inch gauge length and 500 mm/minute grip separation speed. A bundle of 30 fibers is threaded into the grips with care taken to minimize the chance for any contamination. An extrapolated diameter for the fiber bundle is determined from the average diameter of the individual fibers determined via optical microscopy and converted into a theoretical diameter for the fiber bundle as if it were a single fiber. In each experiment, the fiber bundle is stretched until breakage occurs and the software creates a stress-versus-strain plot and calculates the mechanical properties for the sample. Mechanical properties of interest in the study are break stress and percent strain at the break. Five replicates are run and a statistical analysis performed. In each experiment, the fiber is stretched untl breakage occurs and the software creates a stress-versus-strain plot and calculates the desired mechanical properties for the sample. The mechanical properties can include, for example, Young's modulus, stress at break, and percent strain or elongation at break.
EXAMPLES
Various materials were used as components to form thermoplastic compositions and multicomponent fibers in the following Examples. The designation and various properties of these materials are listed in Table 1.
Samples 1 and 2 are poly(lactc acid) (PLA) polymers obtained from Chronopol Inc., Golden, Colo.
A polybutylene succinate (PBS), available from Showa Highpolymer Co., Ltd., Tokyo, Japan, under the designation Bionolle 1020 polybutylene succinate, was obtained.
A polybutylene succinate (PBS) with long chain branching, available from Showa Highpolymer Co., Ltd., Tokyo, Japan, under the designation Bionolle 1903 polybutylene succinate, was obtained.
The wetting agent used throughout the examples was obtained from Petrolite Corporation of Tulsa, Okla., under the designation UNITHOX® 480 ethoxylated alcohol, which exhibited a number average molecular weight of about 2250, an ethoxylate percent of about 80 weight percent, and an HLB value of about 16.
TABLE 1
Weight Number Residual
Melting Average Average Polydisp- Lactic
Material L:D Temp. Molecular Molecular ersity Acid
Designation Ratio (° C.) Weight Weight Index Monomer
PLA Sample 1 100:0 175 187,000 118,000 1.58 <1%
PLA Sample 2 95:5 140-145 190,000 108,000 1.76 <3%
Bionolle 1020 N/A 95 40,000 to 20,000 to ˜2 to ˜3.3 N/A
1,000,000 300,000
Bionolle 1903 N/A 120 40,000 to 20,000 to ˜2 to ˜3.3 N/A
1,000,000 300,000
Example 1
Thermoplastic compositions were prepared using varying amounts of a poly(lactic acid) polymer, a polybutylene succinate, and a wetting agent. To prepare a specific thermoplastic composition, the various components were first dry mixed and then melt blended in a counter-rotating twin screw to provide vigorous mixing of the components. The melt mixing involves partial or complete melting of the components combined with the shearing effect of rotating mixing screws. Such conditions are conducive to optimal blending and even dispersion of the components of the thermoplastic composition. Twin screw extruders such as a Haake Rheocord 90, available from Haake GmbH of Karlsautte, Germany, or a Brabender twin screw mixer (cat no 05-96-000) available from Brabender Instruments of South Hackensack, N.J., or other comparable twin screw extruders, are well suited to this task. The melted composition is cooled following extrusion from the melt mixer on either a liquid cooled roll or surface and/or by forced air passed over the extrudate. The cooled composition is then subsequently pelletized for conversion to fibers.
Converting these resins into fiber and nonwoven was conducted on a in-house 0.75 inch diameter extruder with a 24:1 L:D (length:diameter) ratio screw and three heating zones which feed into a transfer pipe from the extruder to the spin pack, which constitutes the 4th heating zone and contains a 0.62 inch diameter Koch® SMX type static mixer unit, available from Koch Engineering Company Inc. of New York, N.Y., and then into the spinning head (5th heating zone) and through a spin plate which is simply a plate with numerous small holes through which the molten polymer will be extruded through. The spin plate used herein had 15 to 30 holes, where each hole has a 20 mil diameter. The temperature of each heating zone is indicated sequentially under the extrusion temperatures heading in Table 2. The fibers are air quenched using air at a temperature range of 13° C. to 22° C., and drawn down by a mechanical draw roll and passed on to either a winder unit for collection, or to a fiber drawing unit for spunbond formation and bonding, or through accessory equipment for heat setting or other treatment before collection.
The fibers were then evaluated for contact angle and heat shrinkage. The composition of the various fibers and the results of the evaluations are shown in Table 3.
Those skilled in the art will recognize that the present invention is capable of many modifications and variations without departing from the scope thereof. Accordingly, the detailed description and examples set forth above are meant to be illustrative only and are not intended to limit, in any manner, the scope of the invention as set forth in the appended claims.
TABLE 2
Sample # Extrusion Temperatures (° C.)
*1 150/175/155/160/160
*2 180/185/185/190/190
*3 150/155/160/170/170
*4 150/150/160/170/170
*5 15O/150/160/170/170
*6 175/185/190/195/200
*7 170/175/180/185/190
*8 190/205/205/210/210
9 175/185/190/195/200
10 175/185/190/195/200
11 165/175/175/185/185
12 165/175/175/185/185
13 165/175/175/185/185
14 180/190/190/195/200
15 160/165/170/170/175
*Not an example of the present invention.
TABLE 3
Composition of Fiber
Wetting Contact Angle Heat Jet
Sample # PLA Type PLA Wt % PBS Type PBS Wt % Agent Wt % Advancing Receding Shrinkage Stretch
*1 PLA Sample 2 100% 94° 75° 13% 96
*2 Bionolle 1020 100% 93° 60° 0% 96
*3 PLA Sample 2 70% Bionolle 1020 30% 85° 62° 3% 96
*4 PLA Sample 2 85% Bionolle 1020 15% 99° 53° 29% 96
*5 PLA Sample 2 61% Bionolle 1020 26% 13% 97° 48° 2% 96
*6 PLA Sample 1 90% Bionolle 1903 10% 81° 59° 6% 96
*7 PLA Sample 1 100% 84° 66° 27% 96
*8 Bionolle 1903 100% 102° 65° −1% 9.8
9 PLA Sample 1 86% Bionolle 1903 9% 5% 73° 44° 3% 96
10 PLA Sample 1 78% Bionolle 1903 9% 13% 71° 44° −2% 96
11 PLA Sample 1 87% Bionolle 1903 10% 3% 77° 49° 3% 96
12 PLA Sample 1 87% Bionolle 1020 10% 3% 75° 48° 4% 96
13 PLA Sample 1 89% Bionolle 1903 10% 1% 79° 55° 5% 96
14 PLA Sample 1 9% Bionolle 1903 86% 1% 48° 39° 0% 51
15 PLA Sample 1 10% Bionolle 1020 87% 3% 50° 41°
*Not an example of the present invention.

Claims (18)

What is claimed is:
1. A multicomponent fiber prepared from a thermoplastic composition, wherein the thermplastic composition comprises:
a. a poly(lactic acid) polymer in a weight amount that is greater than 0 but less than 100 weight percent,
b. a polymer selected from the group consisting of a polybutylene succinate polymer, a polybutylene succinate adipate polymer, and a mixture of such polymers, in a weight amount that is greater than 0 but less than 100 weight percent,
c. a wetting agent, which exhibits a hydrophilic-lipophilic balance ratio that is between about 10 to about 40, in a weight amount that is greater than 0 to about 15 weight percent, wherein all weight percents are based on the total weight amount of the poly(lactic acid) polymer; the polymer selected from the group consisting of a polybutylene succinate polymer, a polybutylene succinate adipate polymer, and a mixture of such polymers; and the wetting agent present in the thermoplastic composition;
wherein the multicomponent fiber exhibits an Advancing Contact Angle value that is less than about 80 degrees and a Receding Contact Angle value that is less than about 60 degrees.
2. The multicomponent fiber of claim 1 wherein the poly(lactic acid) polymer is present in a weight amount that is between about 5 weight percent to about 95 weight percent, the polymer selected from the group consisting of a polybutylene succinate polymer, a polybutylene succinate adipate polymer, and a mixture of such polymers, is present in a weight amount that is between about 5 weight percent to about 95 weight percent, and the wetting agent is present in a weight amount that is between about 0.5 weight percent to about 15 weight percent.
3. The multicomponent fiber of claim 1 wherein the wetting agent exhibits a hydrophilic-lipophilic balance ratio that is between about 10 to about 20.
4. The mulicomponent fiber of claim 1 wherein the wetting agent is an ethoxylated alcohol.
5. The multicomponent fiber of claim 1 wherein the multicomponent fiber exhibits an Advancing Contact Angle value that is less than about 75 degrees and a Receding Contact Angle value that is less than about 55 degrees.
6. The multicomponent fiber of claim 1 wherein the difference between the Advancing Contact Angle value the Receding Contact Angle value is less than about 30 degrees.
7. The multicomponent fiber of claim 1 wherein the multicomponent fiber exhibits a Heat Shrinkage value that is less than about 15 percent.
8. The multicomponent fiber of claim 1 wherein the poly(lactic acid) polymer is present in a weight amount that is between about 75 weight percent to about 90 weight percent, the polymer selected from the group consisting of a polybutylene succinate polymer, a polybutylene succinate adipate polymer, and a mixture of such polymers, is present in a weight amount that is between about 5 weight percent to about 20 weight percent, the wetting agent is an ethoxylated alcohol, the difference between the Advancing Contact Angle value the Receding Contact Angle value is less than about 30 degrees, and the multicomponent fiber exhibits a Heat Shrinkage value that is less than about 15 percent.
9. A multi-component fiber prepared from a thermoplastic composition blend, wherein the multi-component fiber exhibits an Advancing Contact Angle value that is less than about 80 degrees and a Receding Contact Angle value that is less than about 60 degrees.
10. The multi-component fiber of claim 9, wherein the thermoplastic composition blend comprises from about 5 to about 95 weight percent of a poly(lactic acid) polymer; from about about 5 to about 95 weight percent of a polymer selected from the group consisting of a polybutylene succinate polymer, a polybutylene succinate adipate polymer, and a mixture thereof; and from about 0.5 to about 15 weight percent of a wetting agent, which exhibits a hydrophilic-lipophilic balance ratio that is between about 10 to about 40.
11. The multi-component fiber of claim 10, wherein the thermoplastic composition blend comprises from about 10 to about 90 weight percent of the poly(lactic acid) polymer; from about about 10 to about 90 weight percent of the polymer selected from the group consisting of a polybutylene succinate polymer, a polybutylene succinate adipate polymer, and a mixture thereof; and from about 1 to about 13 weight percent of the wetting agent.
12. The multi-component fiber of claim 10, wherein the wetting agent exhibits a hydrophilic-lipophilic balance ratio that is between about 10 to about 20.
13. The multi-component fiber of claim 10, wherein the wetting agent is an ethoxylated alcohol.
14. The multi-component fiber of claim 10, wherein the thermoplastic composition blend comprises from about 75 to about 90 weight percent of the poly(lactic acid) polymer; from about about 5 to about 20 weight percent of the polymer selected from the group consisting of a polybutylene succinate polymer, a polybutylene succinate adipate polymer and a mixture thereof, and wherein the wetting agent is an ethoxylated alcohol.
15. The multi-component fiber of claim 9, wherein the multi-component fiber exhibits an Advancing Contact Angle value that is less than about 75 degrees and a Receding Contact Angle value that is less than about 55 degrees.
16. The multi-component fiber of claim 9, wherein the difference between the Advancing Contact Angle value and the Receding Contact Angle value is less than about 30 degrees.
17. The multi-component fiber of claim 9, wherein the multi-component fiber exhibits a Heat Shrinkage value that is less than about 15 percent.
18. The multi-component fiber of claim 9, wherein the thermoplastic composition blend comprises from about 75 to about 90 weight percent of a poly(lactic acid) polymer; from about about 5 to about 20 weight percent of a polymer selected from the group consisting of a polybutylene succinate polymer, a polybutylene succinate adipate polymer and a mixture thereof; further wherein the thermoplastic composition blend includes a wetting agent comprising an ethoxylated alcohol; wherein the difference between the Advancing Contact Angle value and the Receding Contact Angle value is less than about 30 degrees; and wherein the multi-component fiber exhibits a Heat Shrinkage value that is less than about 15 percent.
US09/222,094 1997-10-31 1998-12-29 Multicomponent fiber prepared from a thermoplastic composition Expired - Fee Related US6211294B1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US09/222,094 US6211294B1 (en) 1997-10-31 1998-12-29 Multicomponent fiber prepared from a thermoplastic composition
US09/372,019 US6207755B1 (en) 1997-10-31 1999-08-11 Biodegradable thermoplastic composition
US09/436,682 US6201068B1 (en) 1997-10-31 1999-11-09 Biodegradable polylactide nonwovens with improved fluid management properties
US09/437,026 US6268434B1 (en) 1997-10-31 1999-11-09 Biodegradable polylactide nonwovens with improved fluid management properties
US09/606,571 US6475418B1 (en) 1997-10-31 2000-06-29 Methods for making a thermoplastic composition and fibers including same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/962,432 US5910545A (en) 1997-10-31 1997-10-31 Biodegradable thermoplastic composition
US09/222,094 US6211294B1 (en) 1997-10-31 1998-12-29 Multicomponent fiber prepared from a thermoplastic composition

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US08/962,432 Division US5910545A (en) 1997-10-31 1997-10-31 Biodegradable thermoplastic composition

Related Child Applications (3)

Application Number Title Priority Date Filing Date
US09/372,019 Division US6207755B1 (en) 1997-10-31 1999-08-11 Biodegradable thermoplastic composition
US09/436,682 Continuation-In-Part US6201068B1 (en) 1997-10-31 1999-11-09 Biodegradable polylactide nonwovens with improved fluid management properties
US09/437,026 Continuation-In-Part US6268434B1 (en) 1997-10-31 1999-11-09 Biodegradable polylactide nonwovens with improved fluid management properties

Publications (1)

Publication Number Publication Date
US6211294B1 true US6211294B1 (en) 2001-04-03

Family

ID=25505858

Family Applications (3)

Application Number Title Priority Date Filing Date
US08/962,432 Expired - Fee Related US5910545A (en) 1997-10-31 1997-10-31 Biodegradable thermoplastic composition
US09/222,094 Expired - Fee Related US6211294B1 (en) 1997-10-31 1998-12-29 Multicomponent fiber prepared from a thermoplastic composition
US09/372,019 Expired - Fee Related US6207755B1 (en) 1997-10-31 1999-08-11 Biodegradable thermoplastic composition

Family Applications Before (1)

Application Number Title Priority Date Filing Date
US08/962,432 Expired - Fee Related US5910545A (en) 1997-10-31 1997-10-31 Biodegradable thermoplastic composition

Family Applications After (1)

Application Number Title Priority Date Filing Date
US09/372,019 Expired - Fee Related US6207755B1 (en) 1997-10-31 1999-08-11 Biodegradable thermoplastic composition

Country Status (10)

Country Link
US (3) US5910545A (en)
EP (1) EP1025166B1 (en)
JP (1) JP2001521969A (en)
KR (1) KR100552365B1 (en)
AU (1) AU736400B2 (en)
BR (1) BR9813333A (en)
CA (1) CA2307676A1 (en)
DE (1) DE69821381T2 (en)
IL (1) IL135706A0 (en)
WO (1) WO1999023163A1 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060147505A1 (en) * 2004-12-30 2006-07-06 Tanzer Richard W Water-dispersible wet wipe having mixed solvent wetting composition
US7887726B1 (en) * 2006-11-24 2011-02-15 Novana, Inc. Self-reinforced composite made of recycled materials and process of making the same
US20110092939A1 (en) * 2009-10-21 2011-04-21 Donoho Christopher D Disposable diaper with pouches

Families Citing this family (74)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6201068B1 (en) 1997-10-31 2001-03-13 Kimberly-Clark Worldwide, Inc. Biodegradable polylactide nonwovens with improved fluid management properties
US6268434B1 (en) 1997-10-31 2001-07-31 Kimberly Clark Worldwide, Inc. Biodegradable polylactide nonwovens with improved fluid management properties
TW506894B (en) * 1997-12-15 2002-10-21 Ykk Corp A biodegradable resin composition
US6309988B1 (en) 1997-12-22 2001-10-30 Kimberly-Clark Worldwide, Inc. Biodisintegratable nonwovens with improved fluid management properties
US6306782B1 (en) 1997-12-22 2001-10-23 Kimberly-Clark Worldwide, Inc. Disposable absorbent product having biodisintegratable nonwovens with improved fluid management properties
US6544455B1 (en) * 1997-12-22 2003-04-08 Kimberly-Clark Worldwide, Inc. Methods for making a biodegradable thermoplastic composition
RU2002107430A (en) * 1999-08-25 2003-11-10 Кимберли-Кларк Ворлдвайд, Инк. (Us) BIOLOGICALLY DESTRUCTIVE NONWOVEN MATERIALS WITH THE ABILITY TO ABSORBE LIQUID AND CONTAINING THEIR DISPOSABLE ABSORBENT PRODUCTS
WO2001034886A1 (en) * 1999-11-09 2001-05-17 Kimberly-Clark Worldwide, Inc. Biodegradable polylactide nonwovens with fluid management properties and disposable absorbent products containing the same
US6177193B1 (en) * 1999-11-30 2001-01-23 Kimberly-Clark Worldwide, Inc. Biodegradable hydrophilic binder fibers
US6573340B1 (en) 2000-08-23 2003-06-03 Biotec Biologische Naturverpackungen Gmbh & Co. Kg Biodegradable polymer films and sheets suitable for use as laminate coatings as well as wraps and other packaging materials
US7297394B2 (en) 2002-03-01 2007-11-20 Bio-Tec Biologische Naturverpackungen Gmbh & Co. Kg Biodegradable films and sheets suitable for use as coatings, wraps and packaging materials
US7241832B2 (en) * 2002-03-01 2007-07-10 bio-tec Biologische Naturverpackungen GmbH & Co., KG Biodegradable polymer blends for use in making films, sheets and other articles of manufacture
EP1422044B1 (en) * 2001-07-19 2010-10-13 Toyo Seikan Kaisha, Ltd. Molded object obtained through stretching and thermal fixing and process for producing the same
US7172814B2 (en) * 2003-06-03 2007-02-06 Bio-Tec Biologische Naturverpackungen Gmbh & Co Fibrous sheets coated or impregnated with biodegradable polymers or polymers blends
US7368511B2 (en) 2003-12-22 2008-05-06 Eastman Chemical Company Polymer blends with improved rheology and improved unnotched impact strength
US7368503B2 (en) * 2003-12-22 2008-05-06 Eastman Chemical Company Compatibilized blends of biodegradable polymers with improved rheology
US7160977B2 (en) 2003-12-22 2007-01-09 Eastman Chemical Company Polymer blends with improved notched impact strength
US20050282456A1 (en) * 2004-06-17 2005-12-22 The Procter & Gamble Company Laminate comprising a polyhydroxyalkanoate copolymer
CA2571252A1 (en) * 2004-06-23 2006-01-05 Natureworks Llc Injection stretch blow molding process using polylactide resins
CN100564025C (en) * 2004-06-23 2009-12-02 自然工作有限责任公司 Branched polylactic acid polymers and preparation method thereof
DE102004053597B4 (en) * 2004-11-05 2008-05-29 Infineon Technologies Ag A method for automatically generating and / or controlling a telecommunications conference with a plurality of subscribers, telecommunication conference terminal and telecommunication conference server
US8022133B2 (en) * 2005-01-28 2011-09-20 Milliken & Company Co-additive compositions and methods for applying co-additive compositions into nucleated polymer compounds
US20060260031A1 (en) * 2005-05-20 2006-11-23 Conrad Joseph M Iii Potty training device
WO2007070064A1 (en) * 2005-12-15 2007-06-21 Kimberly - Clark Worldwide, Inc. Biodegradable multicomponent fibers
MX2008012848A (en) 2006-04-07 2008-10-13 Kimberly Clark Co Biodegradable nonwoven laminate.
EP2044251B1 (en) 2006-07-14 2019-10-02 NatureWorks LLC Biodegradable aliphatic polyester for use in nonwoven webs
KR101311060B1 (en) * 2006-07-14 2013-09-24 킴벌리-클라크 월드와이드, 인크. Biodegradable aliphatic-aromatic copolyester for use in nonwoven webs
KR101297865B1 (en) * 2006-07-14 2013-08-19 킴벌리-클라크 월드와이드, 인크. Biodegradable polylactic acid for use in nonwoven webs
EP2057209A1 (en) * 2006-08-31 2009-05-13 Kimberly-Clark Worldwide, Inc. Highly breathable biodegradable films
WO2008073099A1 (en) * 2006-12-15 2008-06-19 Kimberly-Clark Worldwide, Inc. Biodegradable polyesters for use in forming fibers
BRPI0622175A2 (en) * 2006-12-15 2011-12-27 Kimberly Clark Co Biodegradable polylactic acids for use in fiber formation
CA2674339A1 (en) * 2006-12-29 2008-07-10 Jayson A. Bexell Flax based fuel pellet and method of manufacture
WO2009024836A1 (en) * 2007-08-22 2009-02-26 Kimberly-Clark Worldwide, Inc. Multicomponent biodegradable filaments and nonwoven webs formed therefrom
EP2065164A1 (en) * 2007-11-27 2009-06-03 Aisapack Holding SA Process of manufacturing a package for hot filling and such a package
KR20100098529A (en) * 2007-12-13 2010-09-07 킴벌리-클라크 월드와이드, 인크. Biodegradable fibers formed from a thermoplastic composition containing polylactic acid and a polyether copolymer
US8227658B2 (en) 2007-12-14 2012-07-24 Kimberly-Clark Worldwide, Inc Film formed from a blend of biodegradable aliphatic-aromatic copolyesters
US7998888B2 (en) * 2008-03-28 2011-08-16 Kimberly-Clark Worldwide, Inc. Thermoplastic starch for use in melt-extruded substrates
US8147965B2 (en) 2008-05-14 2012-04-03 Kimberly-Clark Worldwide, Inc. Water-sensitive film containing thermoplastic polyurethane
US8338508B2 (en) * 2008-05-14 2012-12-25 Kimberly-Clark Worldwide, Inc. Water-sensitive film containing an olefinic elastomer
JP5658560B2 (en) * 2008-05-29 2015-01-28 三菱瓦斯化学株式会社 Composite molded product with two-layer structure
EP2281080B1 (en) * 2008-05-30 2014-03-19 Kimberly-Clark Worldwide, Inc. Nonwoven web comprising polylactic acid fibers
US8470222B2 (en) 2008-06-06 2013-06-25 Kimberly-Clark Worldwide, Inc. Fibers formed from a blend of a modified aliphatic-aromatic copolyester and thermoplastic starch
US8841386B2 (en) 2008-06-10 2014-09-23 Kimberly-Clark Worldwide, Inc. Fibers formed from aromatic polyester and polyether copolymer
US8759279B2 (en) * 2008-06-30 2014-06-24 Kimberly-Clark Worldwide, Inc. Fragranced biodegradable film
US8927617B2 (en) 2008-06-30 2015-01-06 Kimberly-Clark Worldwide, Inc. Fragranced water-sensitive film
US8188185B2 (en) * 2008-06-30 2012-05-29 Kimberly-Clark Worldwide, Inc. Biodegradable packaging film
KR101322099B1 (en) * 2008-07-08 2013-10-25 (주)엘지하우시스 Environmental Friendly Bio-Degradable Materials for Advertising
US8283006B2 (en) * 2008-12-18 2012-10-09 Kimberly-Clark Worldwide, Inc. Injection molding material containing starch and plant protein
US8329601B2 (en) 2008-12-18 2012-12-11 Kimberly-Clark Worldwide, Inc. Biodegradable and renewable film
KR20100097486A (en) * 2009-02-26 2010-09-03 코오롱글로텍주식회사 Biodegradable fiber and preparing thereof, nonwoven made of them
AU2009202397A1 (en) * 2009-06-16 2011-01-06 Because We Care Pty Ltd Biodegradable Polymeric Compositions
WO2011071667A1 (en) * 2009-12-08 2011-06-16 International Paper Company Thermoformed article made from polybutylene succinate (pbs) and modified polybutylene succinage (mpbs)
EP2995642A3 (en) * 2010-06-17 2016-06-15 Tipa Corp. Ltd. Biodegradable sheet comprising polylactic acid and polybutylene succinate adipate, and uses thereof
US8461262B2 (en) 2010-12-07 2013-06-11 Kimberly-Clark Worldwide, Inc. Polylactic acid fibers
EA025062B1 (en) * 2010-12-15 2016-11-30 3М Инновейтив Пропертиз Компани Controlled degradation fibers
GB201105455D0 (en) 2011-03-31 2011-05-18 British American Tobacco Co Blends of a polylactic acid and a water soluble polymer
GB201112402D0 (en) 2011-07-19 2011-08-31 British American Tobacco Co Cellulose acetate compositions
KR101256832B1 (en) 2011-09-21 2013-04-22 주식회사 모아 Resin composition containing recyle polylactic acid and method of manufacturing biodegradable fiber used as reinforcement material in civil enginnering thereby
KR101791049B1 (en) 2011-10-14 2017-11-20 코오롱글로텍주식회사 Functional biodegradable fiber and preparing thereof, nonwoven made of them
CA2859870A1 (en) 2011-12-23 2013-06-27 Solazyme, Inc. Algal thermoplastics, thermosets, paper, adsorbants and absorbants
US20150126091A1 (en) * 2012-04-29 2015-05-07 Nature Works Llc Process for making non-woven fabrics using polylactide resin blends
KR20150023001A (en) 2012-06-13 2015-03-04 티파 코퍼레이션 리미티드 Biodegradable sheet
US20140020165A1 (en) 2012-07-20 2014-01-23 For Kids By Parents, Inc. Potty training device
US9493640B2 (en) 2013-03-15 2016-11-15 Terravia Holdings, Inc. Wood plastic and thermoplastic composites
BR112016028274A2 (en) 2014-06-02 2017-08-22 Procter & Gamble multilayer films of thermoplastic polymer comprising poly (lactic acid)
CN107405900B (en) * 2014-10-27 2021-01-29 蒂帕有限责任公司 Biodegradable sheet
JP6529550B2 (en) * 2016-12-28 2019-06-12 ユニ・チャーム株式会社 Absorbent articles
WO2018124122A1 (en) * 2016-12-28 2018-07-05 ユニ・チャーム株式会社 Absorbent article
WO2018162751A1 (en) * 2017-03-10 2018-09-13 Biome Bioplastics Limited Fabric
GB201704414D0 (en) 2017-03-20 2017-05-03 Biome Bioplastics Ltd Heating apparatus and method
CN109335254B (en) * 2018-10-10 2019-12-20 江苏云之尚节能科技有限公司 Full-degradable heat-preservation environment-friendly fast-transport packaging bag
KR102618136B1 (en) 2020-04-15 2023-12-27 쓰리엠 이노베이티브 프로퍼티즈 캄파니 Compostable compositions, articles, and methods of making compostable articles
KR102395895B1 (en) * 2020-05-26 2022-05-09 도레이첨단소재 주식회사 Biodegradable composite fiber and non-woven fabric including the same
KR102517291B1 (en) * 2021-12-28 2023-04-03 케이에이에프 주식회사 Biodegradable composite fiber and method for manufacturing same

Citations (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3531561A (en) 1965-04-20 1970-09-29 Ethicon Inc Suture preparation
US3792011A (en) 1971-10-14 1974-02-12 Westinghouse Electric Corp Low-cost resinous compositions comprising non-glycidyl ether epoxides
US4367070A (en) 1980-02-21 1983-01-04 Toray Industries, Inc. Process for treating fibrous structure
US4710187A (en) 1985-09-06 1987-12-01 Kimberly-Clark Corporation Form-fitting self-adjusting disposable garment with a stretchable bodyside liner
US4762521A (en) 1986-04-11 1988-08-09 Kimberly-Clark Corporation Absorbent garment with quilted and conformable absorbent pad
US4770656A (en) 1986-12-31 1988-09-13 Kimberly-Clark Corporation Routing of leg elastic to reduce stresses in a stretchable outer diaper cover
US4789592A (en) 1985-09-19 1988-12-06 Chisso Corporation Hot-melt-adhesive composite fiber
US4798603A (en) 1987-10-16 1989-01-17 Kimberly-Clark Corporation Absorbent article having a hydrophobic transport layer
EP0351949A2 (en) 1988-07-20 1990-01-24 International Paper Company Disposable semi-durable nonwoven fabric and related method of manufacture
US5057368A (en) 1989-12-21 1991-10-15 Allied-Signal Filaments having trilobal or quadrilobal cross-sections
US5069970A (en) 1989-01-23 1991-12-03 Allied-Signal Inc. Fibers and filters containing said fibers
US5108820A (en) 1989-04-25 1992-04-28 Mitsui Petrochemical Industries, Ltd. Soft nonwoven fabric of filaments
US5147712A (en) 1990-06-26 1992-09-15 Nippon Unicar Company Limited Non-woven fabric
US5162153A (en) 1991-12-23 1992-11-10 Hoechst Celanese Corporation Poly(butylene terephthalate) copolyester and a process for preparing it
US5202178A (en) 1992-02-28 1993-04-13 International Paper Company High-strength nylon battery separator material and related method of manufacture
US5241066A (en) 1992-06-25 1993-08-31 Basf Corporation Method of recovering caprolactam from mixed waste
EP0569153A2 (en) 1992-05-08 1993-11-10 Showa Highpolymer Co., Ltd. Polyester resin composition
US5273596A (en) 1990-03-21 1993-12-28 Fiberweb North America, Inc. Nonwoven fabric for diaper top sheet and method of making the same
US5277976A (en) 1991-10-07 1994-01-11 Minnesota Mining And Manufacturing Company Oriented profile fibers
JPH06207323A (en) 1993-01-12 1994-07-26 Unitika Ltd Biodegradable latent-crimping conjugate filament and nonwoven fabric made of the filament
JPH06207324A (en) 1993-01-12 1994-07-26 Unitika Ltd Biodegradable conjugate filament and nonwoven fabric made of the filament
JPH06207320A (en) 1993-01-12 1994-07-26 Unitika Ltd Biodegradable conjugate short fiber and its nonwoven fabric
US5336552A (en) 1992-08-26 1994-08-09 Kimberly-Clark Corporation Nonwoven fabric made with multicomponent polymeric strands including a blend of polyolefin and ethylene alkyl acrylate copolymer
JPH06248552A (en) 1993-02-23 1994-09-06 Daiwabo Create Kk Biodegradable fiber composition and hot melt adhesive fiber useful therefor
US5382400A (en) 1992-08-21 1995-01-17 Kimberly-Clark Corporation Nonwoven multicomponent polymeric fabric and method for making same
JPH07133511A (en) 1993-11-10 1995-05-23 Toyobo Co Ltd Biodegradable conjugate yarn and nonwoven fabric using the same
US5508378A (en) 1994-01-21 1996-04-16 Shimadzu Corporation Method for producing polylactic acid
JPH08134723A (en) 1994-11-08 1996-05-28 Unitika Ltd Biodegradable conjugate fiber
US5593778A (en) 1993-09-09 1997-01-14 Kanebo, Ltd. Biodegradable copolyester, molded article produced therefrom and process for producing the molded article
EP0765913A1 (en) 1995-09-29 1997-04-02 Dainippon Ink And Chemicals, Inc. Process for the preparation of lactic acid-based polyester compositions
US5637631A (en) 1994-11-17 1997-06-10 Mitsui Toatsu Chemicals, Inc. Preparation process of degradable polymer
US5691424A (en) 1995-05-25 1997-11-25 Mitsui Toatsu Chemicals, Inc. Heat-resistant molded article of lactic acid-base polymer
US5783504A (en) 1995-04-26 1998-07-21 Fiberweb Nonwoven/film biodegradable composite structure
US5952088A (en) * 1996-12-31 1999-09-14 Kimberly-Clark Worldwide, Inc. Multicomponent fiber

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3906349B2 (en) * 1996-09-27 2007-04-18 東レ・モノフィラメント株式会社 Biodegradable composite monofilament and its use
JPH10110332A (en) * 1996-10-07 1998-04-28 Toray Monofilament Co Ltd Biodegradable monofilament and use thereof
EP0977912B1 (en) * 1997-05-02 2004-09-22 Cargill, Incorporated Degradable polymer fibers; preparation; product; and methods of use

Patent Citations (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3531561A (en) 1965-04-20 1970-09-29 Ethicon Inc Suture preparation
US3792011A (en) 1971-10-14 1974-02-12 Westinghouse Electric Corp Low-cost resinous compositions comprising non-glycidyl ether epoxides
US4367070A (en) 1980-02-21 1983-01-04 Toray Industries, Inc. Process for treating fibrous structure
US4710187A (en) 1985-09-06 1987-12-01 Kimberly-Clark Corporation Form-fitting self-adjusting disposable garment with a stretchable bodyside liner
US4789592A (en) 1985-09-19 1988-12-06 Chisso Corporation Hot-melt-adhesive composite fiber
US4762521A (en) 1986-04-11 1988-08-09 Kimberly-Clark Corporation Absorbent garment with quilted and conformable absorbent pad
US4770656A (en) 1986-12-31 1988-09-13 Kimberly-Clark Corporation Routing of leg elastic to reduce stresses in a stretchable outer diaper cover
US4798603A (en) 1987-10-16 1989-01-17 Kimberly-Clark Corporation Absorbent article having a hydrophobic transport layer
EP0351949A2 (en) 1988-07-20 1990-01-24 International Paper Company Disposable semi-durable nonwoven fabric and related method of manufacture
US5069970A (en) 1989-01-23 1991-12-03 Allied-Signal Inc. Fibers and filters containing said fibers
US5108820A (en) 1989-04-25 1992-04-28 Mitsui Petrochemical Industries, Ltd. Soft nonwoven fabric of filaments
US5057368A (en) 1989-12-21 1991-10-15 Allied-Signal Filaments having trilobal or quadrilobal cross-sections
US5273596A (en) 1990-03-21 1993-12-28 Fiberweb North America, Inc. Nonwoven fabric for diaper top sheet and method of making the same
US5147712A (en) 1990-06-26 1992-09-15 Nippon Unicar Company Limited Non-woven fabric
US5277976A (en) 1991-10-07 1994-01-11 Minnesota Mining And Manufacturing Company Oriented profile fibers
US5162153A (en) 1991-12-23 1992-11-10 Hoechst Celanese Corporation Poly(butylene terephthalate) copolyester and a process for preparing it
US5202178A (en) 1992-02-28 1993-04-13 International Paper Company High-strength nylon battery separator material and related method of manufacture
EP0569153A2 (en) 1992-05-08 1993-11-10 Showa Highpolymer Co., Ltd. Polyester resin composition
US5241066A (en) 1992-06-25 1993-08-31 Basf Corporation Method of recovering caprolactam from mixed waste
US5382400A (en) 1992-08-21 1995-01-17 Kimberly-Clark Corporation Nonwoven multicomponent polymeric fabric and method for making same
US5336552A (en) 1992-08-26 1994-08-09 Kimberly-Clark Corporation Nonwoven fabric made with multicomponent polymeric strands including a blend of polyolefin and ethylene alkyl acrylate copolymer
JPH06207323A (en) 1993-01-12 1994-07-26 Unitika Ltd Biodegradable latent-crimping conjugate filament and nonwoven fabric made of the filament
JPH06207324A (en) 1993-01-12 1994-07-26 Unitika Ltd Biodegradable conjugate filament and nonwoven fabric made of the filament
JPH06207320A (en) 1993-01-12 1994-07-26 Unitika Ltd Biodegradable conjugate short fiber and its nonwoven fabric
JPH06248552A (en) 1993-02-23 1994-09-06 Daiwabo Create Kk Biodegradable fiber composition and hot melt adhesive fiber useful therefor
US5593778A (en) 1993-09-09 1997-01-14 Kanebo, Ltd. Biodegradable copolyester, molded article produced therefrom and process for producing the molded article
JPH07133511A (en) 1993-11-10 1995-05-23 Toyobo Co Ltd Biodegradable conjugate yarn and nonwoven fabric using the same
US5508378A (en) 1994-01-21 1996-04-16 Shimadzu Corporation Method for producing polylactic acid
JPH08134723A (en) 1994-11-08 1996-05-28 Unitika Ltd Biodegradable conjugate fiber
US5637631A (en) 1994-11-17 1997-06-10 Mitsui Toatsu Chemicals, Inc. Preparation process of degradable polymer
US5783504A (en) 1995-04-26 1998-07-21 Fiberweb Nonwoven/film biodegradable composite structure
US5691424A (en) 1995-05-25 1997-11-25 Mitsui Toatsu Chemicals, Inc. Heat-resistant molded article of lactic acid-base polymer
EP0765913A1 (en) 1995-09-29 1997-04-02 Dainippon Ink And Chemicals, Inc. Process for the preparation of lactic acid-based polyester compositions
US5952088A (en) * 1996-12-31 1999-09-14 Kimberly-Clark Worldwide, Inc. Multicomponent fiber

Non-Patent Citations (25)

* Cited by examiner, † Cited by third party
Title
American Society for Testing Materials (ASTM) Designation: D 1238-95, "Standard Test Method for Flow Rates of Thermoplastics by Extrusion Plastometer," pp. 273-281, published Jan. 1996.
Chemical Abstracts 102(10)80131f: Description of Sagatova, M. Sh., D. Shpil'man, and I. Z. Zakirov, "Structural and Mechanical Properties of Fibers Produced From Mixtures of Polyacrylonitrile and Chlorinated Poly(vinyl chloride)," Deposited Doc., 1984, No. Viniti 939-84, 10 pp.
Chemical Abstracts 102(22)186548n: Description of Zakirov, I. Z., M. Sh. Sagatova, and B. E. Geller, "Temperature Transitions in Polyacrylonitrile-Fibroin Mixtures," Vysokomol. Soedin., Ser. B, 1985, vol. 27, No. 2, pp. 116-120.
Chemical Abstracts 105(12)99049u: Description of Zhao Delu, Xue Du, Hungtian Wang, Binghe Li, and Yuanze Xu, "Applications of Controlled Degradation in Polypropylene Tape Yarns," Suliao, 1986, vol. 15, No. 2, pp. 5-10.
Chemical Abstracts 105(26)228372v: Description of Slizite, G., R. Ziemelis, A. Kaziliunas, and A. Paulauskas, "Study of Photochemical Degradation of Articles Produced From Complex Triacetate-Polyamide Fiber," Nauch. Tr. Vuzov LitSSR. Khimiya i Khim. Tekhnol., 1986, No. 27, pp. 98-102.
Chemical Abstracts 106(12)86124K: Description of U, Ju Jui, L. S. Gal'braikh, M. K. Puzdyrev, S. Yu. Kuznetsova, and T. N. Urusova, "Use of a Reactively Dyed Low-Molecular-Weight Polycaproamide For Production of Colored Polypropylene Fibers," Khim. Volokna, 1986, No. 6, pp. 22-24.
Chemical Abstracts 109(4)24162z: Description of Fedorova, R. G., G. I. Kudryavtsev, Z. G. Oprits, O. V. Troitskaya, O. A. Nikitina, A. I. Smirnova, and I. F. Khudoshev, "Composite Fibers From Polyacrylonitrile-Aromatic Polyamic Acid Blends," Khim. Volokna, 1988, No. 2, pp. 11-12.
Chemical Abstracts 114(22)209209s: abstract of laid open Japanese patent application JP 3040865.
Chemical Abstracts 119(12)119421d: abstract of laid open Japanese patent application JP 5093316.
Chemical Abstracts 119(12)119422e: abstract of laid open Japanese patent application JP 5093318.
Chemical Abstracts 119(24)252062d: abstract of laid open Japanese patent application JP 5163616.
Chemical Abstracts 120(8)79336s: abstract of laid open Japanese patent application JP 5093317.
Chemical Abstracts 122(2)12043s: abstract of laid open Japanese patent application JP 6212548.
Chemical Abstracts 122(2)12091f: abstract of laid open Japanese patent application JP 6248515.
Chemical Abstracts 82(14)87465v: Description of Geleji, Frigyes and Gabor Druzsbaczky, "Bicomponent Fiber Structures on Polypropylene Basis," J. Polym. Sci., Polym. Symp., 1973, vol. No. 42, Pt. 2, pp. 713-716.
Chemical Abstracts 88(16)106639x: Description of Fedorova, R. G., G. I. Kudryavtsev, N. V. Yashkova, O. A. Nikitina, M. V. Shablygin, "Structural Thermal Stablilization of Fibers Based on Aromatic and Heterocyclic Polymer Blends," Prepr.-Mezhdunar. Simp. Khim. Voloknam, 2nd, 1977, vol. 4, pp. 36-45.
Chemical Abstracts 96(10)70305j: Description of Gusev, V. K., Z. D. Tul'guk, and R. A. Milivskaya, "Two-Component Acetate Threads," Khim. Volokna, 1981, No. 6, pp. 31-32.
Chemical Abstracts 96(4)21192m: Description of Zakirov, I. Z., "Effect of Small Amounts of Polymeric Additives on Structural-Mechanical and Thermal Properties of Synthetic Fibers Spun By a Wet Method," 3-i Mezhdunar. Simpoz. po Khim. Voloknam, Kalinin, 1981, Kalinin , 1981, No. 5, pp. 105-110.
Chemical Abstracts 99(8)54963d: Description of Dreizenshtok, G. S., A. E. Gal, E. Ya. Sorokin, and K. E. Perepelkin, "Cellulose Decomposition in the Sintering of Fibers From Poly(tetrafluoroethylene) Dispersions," Khim. Volokna, 1983, No. 3, pp. 33-34.
Derwent World Patent Database abstract of EP 640474: Description of H. Utz, "Laminated Film Manufactured By Vacuum Deposition of Functional Layer Between Two Films."
Derwent World Patent Database abstract of JP 6-212511 A: Description of Unitika Ltd., "Biodegradable Staple Fibre Useful For Sanitary Napkin."
Derwent World Patent Database abstract of JP 9-041220 A: Description of Unitika Ltd., "Biodegradable Polyester Fibre."
Good, Robert J. and Robert J. Stromberg, Editors, Surface and Colloid Science-Experimental Methods, vol. II, Plenum Press, 1979, pp. 31-91.
Patent Abstracts of Japan, JP 10-102323 (Toray Monofilament Co., Ltd.) Apr. 21, 1998.
Patent Abstracts of Japan, JP 10-110332 (Toray Monofilament Co., Ltd.) Apr. 28, 1998.

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060147505A1 (en) * 2004-12-30 2006-07-06 Tanzer Richard W Water-dispersible wet wipe having mixed solvent wetting composition
US7887726B1 (en) * 2006-11-24 2011-02-15 Novana, Inc. Self-reinforced composite made of recycled materials and process of making the same
US8465684B1 (en) * 2006-11-24 2013-06-18 Novana, Inc. Self-reinforced composite made of recycled materials and process of making the same
US8992812B1 (en) * 2006-11-24 2015-03-31 Fu-Jya Daniel Tsai Self-reinforced composite made of recycled materials and process of making the same
US20110092939A1 (en) * 2009-10-21 2011-04-21 Donoho Christopher D Disposable diaper with pouches
US8292863B2 (en) 2009-10-21 2012-10-23 Donoho Christopher D Disposable diaper with pouches

Also Published As

Publication number Publication date
WO1999023163A1 (en) 1999-05-14
DE69821381D1 (en) 2004-03-04
EP1025166A1 (en) 2000-08-09
KR100552365B1 (en) 2006-02-20
US6207755B1 (en) 2001-03-27
IL135706A0 (en) 2001-05-20
BR9813333A (en) 2002-02-05
EP1025166B1 (en) 2004-01-28
DE69821381T2 (en) 2004-11-11
US5910545A (en) 1999-06-08
JP2001521969A (en) 2001-11-13
AU736400B2 (en) 2001-07-26
KR20010031625A (en) 2001-04-16
CA2307676A1 (en) 1999-05-14
AU1291099A (en) 1999-05-24

Similar Documents

Publication Publication Date Title
US6211294B1 (en) Multicomponent fiber prepared from a thermoplastic composition
US5952088A (en) Multicomponent fiber
US6201068B1 (en) Biodegradable polylactide nonwovens with improved fluid management properties
US6197237B1 (en) Method of making a multicomponent fiber and nonwoven web containing the same
US6544455B1 (en) Methods for making a biodegradable thermoplastic composition
AU772567B2 (en) Biodisintegratable nonwovens with fluid management properties and disposable absorbent products containing same
US6110849A (en) Thermoplastic composition including polyethylene oxide
US6268434B1 (en) Biodegradable polylactide nonwovens with improved fluid management properties
WO2001034886A1 (en) Biodegradable polylactide nonwovens with fluid management properties and disposable absorbent products containing the same
US6306782B1 (en) Disposable absorbent product having biodisintegratable nonwovens with improved fluid management properties
US6309988B1 (en) Biodisintegratable nonwovens with improved fluid management properties
WO1998029493A1 (en) Thermoplastic composition
EP0951504B1 (en) Thermoplastic composition
MXPA99006199A (en) Multicomponent fiber
ZA200200663B (en) Biodisintegratable nonwovens with fluid management properties and disposable absorbent products containing same.

Legal Events

Date Code Title Description
CC Certificate of correction
FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

Free format text: PAYER NUMBER DE-ASSIGNED (ORIGINAL EVENT CODE: RMPN); ENTITY STATUS OF PATENT OWNER: LARGE ENTITY

FPAY Fee payment

Year of fee payment: 4

REMI Maintenance fee reminder mailed
LAPS Lapse for failure to pay maintenance fees
STCH Information on status: patent discontinuation

Free format text: PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362

FP Lapsed due to failure to pay maintenance fee

Effective date: 20090403